| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs377408497 | snp | A/G/T | 0.02016 | 0.0983543 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999693 | CATGGCCCCGGCCTC[A/G/T]GCTGTCCCCTGGGCA | 79058 |
| rs377422140 | in-del | -/GCAC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985264 | TATGCACACACGCAC[-/GCAC]ACCTGCACATACCTG | 79058 |
| rs377435227 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000698 | TCCTCGGCCGAGACC[C/T]GGGGTGGTTCACAGA | 79058 |
| rs377436250 | snp | A/G | 0.000260745 | 0.0114151 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009069 | CGTGGACCGGGAGCC[A/G]GTGGTGTGCCACCCC | 79058 |
| rs377488610 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995425 | ATGAGCCACGGGGCT[C/T]AGGACCCAGGCCCAG | 79058 |
| rs377549074 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998937 | GTGGCTGTGGCCTGA[C/T]CCTCTCCCTCACGCC | 79058 |
| rs377551534 | snp | A/C | 4.99954e-05 | 0.00499952 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994804 | GGTACCTGATGGTTT[A/C]TTTCCTCTCCTCCCA | 79058 |
| rs377590408 | snp | C/T | 6.16314e-05 | 0.00555085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995032 | AAAAGAGGGAGTGGC[C/T]GGCCCTCGGAGCCCG | 79058 |
| rs377597070 | snp | C/G | 1.65965e-05 | 0.00288062 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011586 | CCACCTGGGGAACCC[C/G]GAGCTGTCATTTTAC | 79058 |
| rs377659219 | snp | A/G | 3.69638e-05 | 0.0042989 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996401 | CAAGGTGCTTCCCTT[A/G]TCCTCTGGCCCCACT | 79058 |
| rs386386775 | in-del | -/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975781 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 79058 |
| rs386799929 | multinucleotide-polymorphism | GT/TC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985969 | GGATGGGATCATAAG[GT/TC]CTCTTTTTTTTAAGA | 79058 |
| rs527270564 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995696 | ACCAGGGCTTCCTCC[A/T]TGCAGCCCAGCTCTG | 79058 |
| rs527296268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999086 | TCCTCAGCTTCCTCA[C/T]CTGCAGAACTAAGGT | 79058 |
| rs527394841 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985224 | TGCACACAACTGCAC[A/C]CCCCCGCACACACCC | 79058 |
| rs527418859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990405 | CCCTATAGTCTGAAG[G/T]TTCTGCCCAGCACAG | 79058 |
| rs527547530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980710 | TTTACACCGAATGGG[C/G]TGGCTGATACAGACG | 79058 |
| rs527585287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981351 | TCAGTTGGTTGGGGG[A/G]GGCTTAGGGTTTCAT | 79058 |
| rs527623198 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006128 | CCTTGCGGGTACACA[C/T]GCGTGCTTGGGGTGT | 79058 |
| rs527638701 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82018060 | CTACCCTTTCCCCTC[C/T]CTGCACGGGGCTCCA | 79058 |
| rs527654671 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984094 | CTGACCTCATGATCT[A/C]CCCGCCTCGGCCTCC | 79058 |
| rs527762452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014402 | TGCAGCCCCCACTCC[C/T]GCTCTGTGGGTGGAT | 79058 |
| rs527786205 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979030 | GAGCCTGCATTTGTT[G/T]CGGGGACCGTCCATA | 79058 |
| rs527824542 | snp | C/T | 0.000795229 | 0.0199244 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010002 | GCAAGCTCCGCCTCC[C/T]GGGTTCAAGTGGTTC | 79058 |
| rs527889588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010305 | GAGGCCAAGGTGGGC[A/G]GATCATGAGGTCAGG | 79058 |
| rs527961867 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982145 | GGCTAATTTTTGTAT[A/T]TTTAGTAGAGACGGA | 79058 |
| rs527992440 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987101 | AGCAAAGCGAAGCCA[C/T]GGGCAGGGGTGAGCG | 79058 |
| rs528005910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999563 | ACCCGGGAGGCGGAG[A/G]TTGCAGTGAGCCGAG | 79058 |
| rs528033238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013063 | GAGGTGAGAAGCTTG[C/T]TCACTGCCTGGGGCT | 79058 |
| rs528066766 | snp | C/T | 0.00185701 | 0.0304147 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977628 | ACGCCGGCCCGGCGG[C/T]GGGTCACGTGAGCGG | 79058 |
| rs528114039 | snp | A/G | 0.000144791 | 0.00850733 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009047 | TCCAGCCCGTGGACC[A/G]GGAGCCCGTGGACCG | 79058 |
| rs528178909 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003739 | CTGTCCACGCCGGTC[A/G]CAGCGGTCTCCCCAC | 79058 |
| rs528243317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004274 | CGCAGGGCTGCCCCC[A/G]GCATCCCGGACAGCG | 79058 |
| rs528284919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998107 | GCTGGGATTACAGGC[A/T]TGAGCCACCGCGCCC | 79058 |
| rs528321753 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991841 | ACCTGTGTTTGCGCC[C/T]GGCTTTGTCATACCC | 79058 |
| rs528358101 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010326 | TGAGGTCAGGAGATC[C/G]AGACCATCCTGGCTG | 79058 |
| rs528406057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988759 | CGTCGTGTGGGTGTC[A/G]TGTGGGTGTTGCGGG | 79058 |
| rs528557549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991969 | TGGTGCATAAAGAAT[A/G]TGCCCTCGAAGCCAG | 79058 |
| rs528661979 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004381 | GTTAGCATCATTGTG[A/G]TCCGGTCCTTGGCGG | 79058 |
| rs528674647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006551 | TGTCTCTCTCCTTGC[C/T]TCCTGCTCCTCCTCC | 79058 |
| rs528701591 | snp | C/T | 4.44949e-05 | 0.00471651 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017120 | AGCTGCCGGGTACTG[C/T]GGCTGGGTGGAAGGT | 79058 |
| rs528732954 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981474 | ACCTCTGTCTCCCAG[A/G]TTCAAGTGATTCTTC | 79058 |
| rs528762575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012460 | AAGTTGCTTCTGACA[C/T]GGCTTTCCGGCCTCC | 79058 |
| rs528783423 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976910 | GTTTCCTGAGGCTGC[C/G]ACCAAGCCCCTCCTC | 79058 |
| rs528834931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008551 | GACGCTGTCCCTCCC[A/G]CATCCCAGGGTGGGC | 79058 |
| rs528854144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991425 | AGCCCTCTGGGTGTG[C/T]TGGGGTGTAGGGATG | 79058 |
| rs528860301 | snp | C/T | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017554 | TGCATCCTGAACCCG[C/T]GTGGGTCTCCTCTTC | 79058 |
| rs528915094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015711 | GAGGCCCGGTGGTGG[C/T]GGAGCATGCTCTCCA | 79058 |
| rs528921970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986645 | GTTCTCGCCCTCCCC[A/G]GGCCTCAGTTTCCTC | 79058 |
| rs528928460 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006675 | AGGCTGGGGAGGGGG[G/T]ACGGGAATTCCCCCA | 79058 |
| rs528949653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981491 | TCAAGTGATTCTTCT[A/G]CCTCAGCCTCCCGAG | 79058 |
| rs528986793 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982138 | CATGCCTGGCTAATT[G/T]TTGTATTTTTAGTAG | 79058 |
| rs529043051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011391 | GGTGGCCCAGCCACG[C/G]CGAGCACCTGGAGTG | 79058 |
| rs529052610 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992871 | ACCCGCCGTGTGTGT[C/G]GTGCGCACGTGCTCC | 79058 |
| rs529076151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007315 | AGGCCCTTGGGATGA[C/T]GGGTAGGAATCTAGG | 79058 |
| rs529090430 | in-del | -/AG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995020 | GTGTTTCATGGAAAA[-/AG]AGGGAGTGGCCGGCC | 79058 |
| rs529096868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011940 | TGGGTGGACAGGGAG[A/T]GGCTGGCCTCCCTTG | 79058 |
| rs529104796 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976137 | CTTGACCATGGAGGA[A/C]TTCAGCAGACCCAAA | 79058 |
| rs529167765 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998924 | AGCATGCCTGTGTGT[C/G]GCTGTGGCCTGACCC | 79058 |
| rs529199628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002077 | CAGGGGCACAATTAC[A/G]GCTCACAGCAGTCAT | 79058 |
| rs529262574 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010340 | CGAGACCATCCTGGC[C/T]GACACGGTGAAACCC | 79058 |
| rs529275315 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002814 | TGCCTGCTTTGGCCT[-/C]CCCAAATTGTTAGGA | 79058 |
| rs529284413 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987122 | GGGGTGAGCGGGACC[C/T]GAGGCAGGAGGTGAC | 79058 |
| rs529304574 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012443 | GGGGCCGTGCGCCTC[A/T]GAAGTTGCTTCTGAC | 79058 |
| rs529325253 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010399 | TCAGGAGAGGTGGCG[C/G]ACGCCTGTAGTCCCA | 79058 |
| rs529393406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006109 | CTTGGGGGCGTGTGT[A/G]TGTCCTTGCGGGTAC | 79058 |
| rs529415593 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000275 | GGGCTCGCAGCCCAG[A/T]GTAGTGCCCGCCCGT | 79058 |
| rs529561621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995243 | GTCCCTGGCCTCACA[A/G]GGGCCTTTTGTTTCC | 79058 |
| rs529577283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990933 | CAGGCGGGCGAGTCC[C/T]GTAGTTTGAATCCCA | 79058 |
| rs529767824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999457 | CATGGCAAAACCCTG[C/T]CTCTACCAAAAATAC | 79058 |
| rs529847050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994169 | TGGGAGGCGTGCTGC[A/G]TATACCTGCCCACCC | 79058 |
| rs529847358 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989433 | GTCCCTGCACTGGCC[A/C]AGGAGGCTTGGGGAG | 79058 |
| rs529910329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989932 | AGCTGGGATTACTGG[C/T]GCACGCCATCACGCC | 79058 |
| rs529913341 | snp | C/G/T | 0.00199529 | 0.0315338 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985163 | ACGCACATGCGCACA[C/G/T]CTGCACACACCCACA | 79058 |
| rs530030790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988343 | GCTCATGCTTGTAGT[C/T]CCAGCTACTCAGGAG | 79058 |
| rs530091537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988746 | AGCCATGCTCTTCCG[C/T]CGTGTGGGTGTCATG | 79058 |
| rs530135764 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017995 | GGCTGGGTCGCCTCC[A/G]ATGGTTCCCAGGGGC | 79058 |
| rs530142280 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017569 | CGTGGGTCTCCTCTT[C/G]GTTTTTAACCTAACA | 79058 |
| rs530143985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984015 | GCCCGCCACCACACC[C/T]GGCTAATTTTTGTAT | 79058 |
| rs530254993 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014308 | GCCCCCTTCCTTCCA[C/T]CCACCAGGCCCTACC | 79058 |
| rs530255088 | snp | A/G | 0.000126695 | 0.00795809 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009580 | AAGGTCTGCAGACAG[A/G]ATGTGGGGGCGACTG | 79058 |
| rs530314250 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990589 | CGCCGAGCTCTGGGG[A/G]ACACTGCTCTCTGCC | 79058 |
| rs530316175 | snp | C/T | 0.0350765 | 0.127702 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009887 | AGTGGCCAGTTGATC[C/T]TCCCCTGCTCATGAT | 79058 |
| rs530371036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005040 | CATCCGTGGCTGGGC[A/G]AGGGTCAGCTGCCAT | 79058 |
| rs530402507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004581 | ATGGTGCCAGCTGGA[C/T]CCTCCACGCTCCTTG | 79058 |
| rs530420525 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983177 | TGGCTCCAGCCGTGA[C/T]GGCCGGGGTCTGTGA | 79058 |
| rs530457390 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976766 | ACGTGCGAGTGCTGT[C/T]CATGAGTGGCCCAGG | 79058 |
| rs530481067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012103 | AGTGTGGGCACAGGG[C/T]GTGCTCGTGAGGGGC | 79058 |
| rs530543528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012437 | TCCGAGGGGGCCGTG[C/T]GCCTCTGAAGTTGCT | 79058 |
| rs530627371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003702 | CTTCAGAGGCAGTCC[C/T]GCCTGCGTCCTTTGT | 79058 |
| rs530676048 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003124 | AAGAGCTGGCATTAC[A/C]GGCGTGAGCCACCGT | 79058 |
| rs530686063 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992414 | CCGCACATCAAAGCC[A/G]GGCTGGCGTTTGATG | 79058 |
| rs530741980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996948 | GCGTGGCCGTGATGC[A/G]GGCAGAGGAACCCAA | 79058 |
| rs530783596 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987326 | AAGCAGGGATCCCGG[C/T]GCCCTGGCTCTGTGC | 79058 |
| rs530834760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004987 | CCTGCTGCCCGGGGC[C/T]GGGGGTCTGGGCCTC | 79058 |
| rs530873534 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007037 | CCCTGGCATCTCCCT[A/C]TGTCATTTGGTGGCC | 79058 |
| rs530938487 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001482 | GAATGGCCACCAAGC[A/G]TGGCTGGCAGATGGC | 79058 |
| rs530993837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986824 | GTCTGACAGTAGTGC[C/T]GCGCTGCATGGCACG | 79058 |
| rs531045247 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984597 | AAAAAAAAAAAAGAG[C/T]AGCAAACATTTACCA | 79058 |
| rs531056515 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996355 | GAGGGTGAGCCTGGG[C/G]CGGGAGAGGGTGAGC | 79058 |
| rs531056920 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991562 | CCCTGTCCATCCCTG[C/T]CCGTCCCTGTTCATC | 79058 |
| rs531127682 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987520 | GGCCGTCCTCCCTGG[C/T]TGTGCTGTCAGTCCT | 79058 |
| rs531189801 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987138 | GAGGCAGGAGGTGAC[A/G]GAGCCTAAGAGCAAA | 79058 |
| rs531233905 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016655 | GAGATCTGCGGCCCC[C/T]AGTAACCACCTCCCC | 79058 |
| rs531263427 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995362 | TTTGGAAGCTCCCTG[G/T]CTGGGGCTGTGACGG | 79058 |
| rs531278475 | snp | G/T | 3.31603e-05 | 0.00407174 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985521 | GGTTCGCATCGCTTT[G/T]CAGCTGGACGATGGC | 79058 |
| rs531424612 | snp | A/G | 6.68349e-05 | 0.0057804 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010860 | GCTTCTTCCGCCCCA[A/G]CGAGACAGGTGGGCA | 79058 |
| rs531444943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986024 | ACCTAGGCTGCTCTT[A/G]AACCCATGGGCTCAA | 79058 |
| rs531487968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011371 | GTCCCAAGTGTGGCC[C/T]GCACGGTGGCCCAGC | 79058 |
| rs531529289 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981410 | TTGAGGTGGAGTCTC[A/G/T]CTCTGTCACACAGGC | 79058 |
| rs531553262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001036 | CCTTGCTCCTGGAGC[C/T]GGGGCCTGGGGTTTC | 79058 |
| rs531595718 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979069 | TTGTGCTTGGCTTTG[C/G/T]CTGGGCAGAGCCACC | 79058 |
| rs531631009 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979798 | TGGATCCCTGCAGTC[C/T]CACAGCCCCTGGAAT | 79058 |
| rs531672474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007204 | TGCCCAGGTGAAGGG[C/T]GGGTGTGGGAGGTTT | 79058 |
| rs531688038 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010325 | ATGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 79058 |
| rs531690151 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014462 | GTGCCTTCTCTCTCC[C/T]GGGCACCGTGGTGCC | 79058 |
| rs531754139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005672 | CCAGGTGGGGATGTT[C/T]GTAGGGACAGTGGTA | 79058 |
| rs531910625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994755 | CCGAGTCTCCTGCCC[C/T]AGGGCCTCCGTGGCA | 79058 |
| rs531937702 | snp | C/T | 0.021333 | 0.101051 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006102 | GTGTGTGCTTGGGGG[C/T]GTGTGTGTGTCCTTG | 79058 |
| rs531999280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000243 | TCTTGTCTGCAGAGC[A/G]TGGGGCGTGGAGCAT | 79058 |
| rs532137213 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978487 | GCCGAGATCGCGCTA[C/G]TGCACTCCAGCCTGG | 79058 |
| rs532260890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989357 | GAGTGCCTGGTGGGC[C/T]CTCTGCTGGGAGCTG | 79058 |
| rs532275306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993370 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 79058 |
| rs532314825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984682 | TCCTGAGGCTGCAGT[C/T]AGGTTCGGTGGAGCT | 79058 |
| rs532326403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988932 | TCATTTCCAGGCCGG[A/G]CATGGCGGCTCTCAC | 79058 |
| rs532338354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993717 | TGACCCTCCCAGTAC[C/T]CCCCATCCCGGAGGG | 79058 |
| rs532452965 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992847 | TGTCCCAGCCTGTGC[A/G]CAGAGGACACCCGCC | 79058 |
| rs532457952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017216 | CTAGGTGCTGTGGCC[A/G]GCAGGGCCGAGTGCT | 79058 |
| rs532590333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987741 | GCTTTGGAGCTGGCT[G/T]TGGTGGTGGCTGTGG | 79058 |
| rs532750385 | snp | A/G | 0.000310207 | 0.0124502 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983676 | AGAACATGGTGGGTC[A/G]TGCTCTGGGGGAGGC | 79058 |
| rs532787592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977893 | GCGGCCCCGCCCCCT[G/T]CTCGCCGTCACCTGC | 79058 |
| rs532790060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987076 | GAGGCAGGAGATGAC[A/G]GAGCCTAAGAGCAAA | 79058 |
| rs532809081 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976138 | TTGACCATGGAGGAA[C/T]TCAGCAGACCCAAAG | 79058 |
| rs532823928 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975595 | TGGGATTACAGGCAC[A/G]CACCGCCATGCCCGG | 79058 |
| rs532880928 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978418 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 79058 |
| rs532882646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003843 | TCCGCCGCCTGCCTC[C/T]GAGGGTGGCCGGGGC | 79058 |
| rs532909914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016288 | CGCTGGTCCCAGGAC[A/G]CCCTGGCCTTGCTTA | 79058 |
| rs532965465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002290 | TTTTGAGACAGTCTC[A/G]CGCTGTCACCCAGGC | 79058 |
| rs533030061 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976155 | CAGCAGACCCAAAGC[C/T]GACCAAGTGGTTCAA | 79058 |
| rs533080794 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006420 | GCGGAAGGAAAGTGA[A/G]TGCAGCCGAATGATC | 79058 |
| rs533082531 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013653 | CCGGCCCCCGGCTTC[C/T]GAGAGGGACAGCGTG | 79058 |
| rs533116219 | in-del | -/GAGC | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991925 | AGCCGCGCCTTGCCG[-/GAGC]GAGCGGGGCCCCAGC | 79058 |
| rs533138341 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993371 | GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT | 79058 |
| rs533208091 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992574 | CCTCATGACCATCTC[C/T]GGACCCCTGGCCATC | 79058 |
| rs533220407 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002912 | CAGGGTCTGTCTATG[C/T]TGCCTAGCCTGGAGT | 79058 |
| rs533352375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990979 | TAGTTGCCAAGTGGT[A/G]AAAGGCAGGGGTGTG | 79058 |
| rs533364144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006476 | TTGTGTCTGCCCATC[C/T]TTCTGTGGGCTGAAA | 79058 |
| rs533493599 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001329 | GCCCCCACATCCGAC[A/G]CGGTGCAGACTCCCA | 79058 |
| rs533495332 | in-del | -/TAG | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003300 | AGGAAATTTAAAAAT[-/TAG]TAGGGCGTGATGGTG | 79058 |
| rs533554498 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995783 | CACGGTCAGGCATGG[G/T]CAGCAGGTCCTGCCC | 79058 |
| rs533626078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991519 | GTCTGTGCATGCTGC[C/T]GGGCCAGCTCAGAGC | 79058 |
| rs533639445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014563 | TGTGGTGCCGCCTTC[C/T]TCCCGGGCACGGTGG | 79058 |
| rs533690671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986776 | GACTGTGCGTTGGGC[A/G]CGCTTGGTGGCCCCA | 79058 |
| rs533699676 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010237 | GAATGAAACTTTAAA[C/G]AGCACATTTGAGCCG | 79058 |
| rs533757651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984343 | AGCACTTTAGGAGGC[C/T]GAGGCGGGCAGATCA | 79058 |
| rs533847616 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984986 | CACACCCACACACCT[A/G]CGTGCACACCCCCCC | 79058 |
| rs533916768 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978066 | GCCGGGAAGAGGGAG[A/G]AGTGGAGCCCTAGAC | 79058 |
| rs533942552 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014704 | GGGGGCGGCCAGGCG[C/G/T]TGGGCCACGTGTGCA | 79058 |
| rs533956797 | snp | A/G | 2.31008e-05 | 0.00339851 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009185 | TGGCCCAGCTCAAGA[A/G]TGAGCGGTGGGTGCC | 79058 |
| rs533995087 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005273 | GGAAACATGAGGCCG[C/T]GTGAAGTGGGCATCA | 79058 |
| rs534006207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004028 | ACAAACCCTCAGAGA[C/T]GCTGGAAACTCTGAG | 79058 |
| rs534008960 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010344 | ACCATCCTGGCTGAC[A/G]CGGTGAAACCCCATC | 79058 |
| rs534055381 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005851 | AGCGTGACCGTGTGT[C/G]TGGGAAAACCGTCCG | 79058 |
| rs534066494 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004635 | CCACAGGCACCCCCA[A/C]CCTGTGGCGCATTTT | 79058 |
| rs534120127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999851 | CCGGGCGTCTGCACC[A/G]TGTTGGATGTGGGGG | 79058 |
| rs534128798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998212 | CTGGGCTCAAGCGAT[C/T]TTCTTATCTCAGCCA | 79058 |
| rs534130712 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992017 | CCCTCCTGGCCGTCC[C/T]GCTGGCTTCTGGCCC | 79058 |
| rs534169464 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984680 | TGTCCTGAGGCTGCA[A/G]TCAGGTTCGGTGGAG | 79058 |
| rs534189651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993456 | CTGACCTCGTGATCC[A/G]CCCATCTCGGCCTCC | 79058 |
| rs534251843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989065 | ATACAAAAAGCAGCT[A/G]GGTGTGGTGGTGAGG | 79058 |
| rs534275764 | in-del | -/GT/GTGT | 0.0162516 | 0.088765 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006300 | CGTGCGTGTTTGGGG[-/GT/GTGT]GTGTGTGTGTGTCCT | 79058 |
| rs534280908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009696 | GTCTGTGGACAGGAC[A/G]TGGTGGCGACTGAGG | 79058 |
| rs534334526 | in-del | -/CTGTGG | 0.00716266 | 0.059414 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001080 | CTCACACCCGGCCCT[-/CTGTGG]CTGACAGCCGGTGTG | 79058 |
| rs534382811 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007774 | CCCGGGAACCCAGGC[C/G]TGCTCGCGGCCCTCT | 79058 |
| rs534468192 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992503 | GCCGGGGAAGGACTG[C/T]GAGTTGGGACTCTGG | 79058 |
| rs534521654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987804 | GTGAGCCGAGATCGC[A/G]CCATTGCACTCTAGC | 79058 |
| rs534533046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993862 | CATAGGGCCTGGCAG[C/G]GCACCTGCATGACCT | 79058 |
| rs534547450 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994133 | CCCGTCTCCCGGGCT[G/T]CCATGCACATCAGGC | 79058 |
| rs534556611 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983436 | GGAGCTGCCACAGGA[A/C]GTGGATGGCGGGGCG | 79058 |
| rs534576097 | in-del | -/TCTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982744 | TTCTTTCTTGTTTTC[-/TCTT]TCTTTCTTTCTTTCT | 79058 |
| rs534579518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988412 | GTGAGCTGAGATTGC[A/G]CCACTGCACTCCAGC | 79058 |
| rs534604496 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003266 | GCCTGGGCAACATAA[C/T]GAGACCCCATCTCTA | 79058 |
| rs534638610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983810 | TTCCCTGGGTTGGGC[C/G]CAAACAGCTTCCTGT | 79058 |
| rs534797043 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005408 | GGGTCGGCAGGTCTC[C/G]TGAGAGGCCTCATCT | 79058 |
| rs534836703 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008431 | TGCTGAGGTGTCCCA[C/G]GTACCCCAGCACTGT | 79058 |
| rs534842689 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979902 | AGCAGAAGGGTCAGA[A/G]CCCTCATATGGATAG | 79058 |
| rs534843978 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001836 | GGATGACCCCCCTCA[C/T]CAAACTGCTTTTCCT | 79058 |
| rs534861579 | in-del | -/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006214 | TGCATGTGCACAGGT[-/GT]GTGTGTGTGTGTGTG | 79058 |
| rs534922724 | snp | A/C/T | 2.33522e-05 | 0.00341695 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012143 | CCACTTGAGGCGTCA[A/C/T]CCCCATCTGCAGGCC | 79058 |
| rs534956256 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977391 | ACCGCGCGCCCAGCC[C/T]CGGCCCAGCCTGGCC | 79058 |
| rs535028982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991585 | TGTTCATCCCTGTCC[A/G]TCCTTGTCCATTCCT | 79058 |
| rs535029422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986548 | TTGGGTCTTTTCATC[A/G]TTGGCTGGAAGTCTC | 79058 |
| rs535041735 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000288 | AGAGTAGTGCCCGCC[C/T]GTGCTCGCCCGTCGG | 79058 |
| rs535071161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986955 | CCCTGGAGATGGCAG[C/T]GGGTTAAGCACGAGC | 79058 |
| rs535096879 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010485 | AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 79058 |
| rs535111198 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016430 | CTTCACAGCAGGGGG[A/C/G]TGCTCTGCCCACACC | 79058 |
| rs535127957 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988210 | TCACGCCTGTAATTC[C/T]AACCCTTTGGGAGGC | 79058 |
| rs535138609 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991063 | GTGACCGAGACCTGC[C/T]GTGGAACGATGCCAA | 79058 |
| rs535173971 | snp | C/G | 1.67928e-05 | 0.0028976 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011650 | CCTCCAGTGCTCGGG[C/G]CCTTGGTGCTGTGGG | 79058 |
| rs535174123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010971 | AGCCACCTGGCCTGC[A/G]GGCTCCAGGGCACTG | 79058 |
| rs535174259 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006268 | CTTGGGGGGCGTGTG[C/T]GTGTCCTTGCGGGTG | 79058 |
| rs535249408 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007548 | GGCTGTGCCCTGGAC[A/G]TGGCCGCCTGAGCAC | 79058 |
| rs535256146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000521 | TTTCAGTGATGGGGG[A/G]AGGGGAGAAGGGAAC | 79058 |
| rs535315285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008254 | CAGGGTAGACGGGAC[A/G]GGACCAGGAGGGTTG | 79058 |
| rs535381226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002702 | TGAGTAGCTAAGAGG[C/T]GCCTGCCACCATGCC | 79058 |
| rs535384652 | snp | A/G | 3.84689e-05 | 0.00438554 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015350 | CAAGCACGTGGGGAC[A/G]GGCCGGGTAGGCTGC | 79058 |
| rs535432773 | snp | A/G/T | 2.77273e-05 | 0.00372329 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995954 | GGGCTCTGGGGTCCC[A/G/T]GTGCAAGGCGCACCT | 79058 |
| rs535439608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980063 | TCTTGGCTCACTGCA[A/G]CCTCCACCTCCTAGG | 79058 |
| rs535663084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990097 | CACTTTTTCTTGTAA[C/T]CGCATTAAAGAAGAA | 79058 |
| rs535704196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985301 | ACTCACATGCACACA[C/T]GCATGCTGGTGCAGC | 79058 |
| rs535726803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995491 | CACCCTTTGGCTTTT[C/G]TGCTGGGCCATTGAC | 79058 |
| rs535796938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991265 | GGCCCCCAGTGTGCC[C/T]GGCCCCTGGCTGGAT | 79058 |
| rs535812059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980224 | CTGACCTTGTGATCC[A/G]CCTGCCTTGGCCTCC | 79058 |
| rs535826440 | in-del | -/CA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984853 | CCCCTGCACACACCC[-/CA]CACACACCTGCACAC | 79058 |
| rs535931661 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999798 | GCAACCTCATGCCTC[A/C]CTCTTGCCTCCCGGC | 79058 |
| rs535992440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994342 | TCGGTGACATCAGGC[A/G]TCGGCTTTGAAGGAG | 79058 |
| rs536004222 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984292 | TGTTAGAGCCGAAAG[C/T]GCTGCATGGATGCCG | 79058 |
| rs536030451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014156 | ACTCACCTGGCAGGG[C/T]GTGACTGGCACTTCT | 79058 |
| rs536199160 | in-del | -/AC | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985074 | CACGCACACACCTGT[-/AC]ACACACACCTACACA | 79058 |
| rs536223495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017238 | CCGAGTGCTTCAGCC[A/G]GGCTGGTGGGCGGGT | 79058 |
| rs536231746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983407 | CTCTGCAGGTCATGA[C/T]GTCCCGCTGTTGGGG | 79058 |
| rs536262495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988546 | TTGGTGGTAAAGCCC[A/G]GAGCCCCCAGCCTGC | 79058 |
| rs536278952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012526 | TGCTAGGCGGCCTGC[C/T]TGAACTGAGGCCGCT | 79058 |
| rs536298255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983889 | TTGAGCTGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 79058 |
| rs536323800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988998 | GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG | 79058 |
| rs536342274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013330 | TGCCCAGGCCTGCAG[C/T]CCACCCTCCCGCTGG | 79058 |
| rs536405216 | snp | C/T | 6.8734e-05 | 0.00586194 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009153 | TGAGCTGACGGTGGA[C/T]GACGTGAGAAGACGC | 79058 |
| rs536418689 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010527 | GAGTGAGACTCCATC[-/T]CAAAAAAAAAAAAAA | 79058 |
| rs536425433 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984849 | CACACCCCTGCACAC[A/C]CCCCACACACACCTG | 79058 |
| rs536470631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003935 | TCCAGGGGAAACTCC[A/G]CACTCCCTCTCACCG | 79058 |
| rs536481331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014524 | CCTCCCGGGCTCTGT[A/G]GTGCCATCTCCCTGC | 79058 |
| rs536531904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997824 | ACCTTTACTGAGGCA[C/T]CCACTTTTTTTTTTT | 79058 |
| rs536730317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002368 | GTTCAAGTAATTTTT[C/G]TGCCTCAGCCTCCCG | 79058 |
| rs536732020 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996235 | TGGGGGCTGGGCTGC[A/C]CCGACCTCATCTCTG | 79058 |
| rs536755875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977952 | GGGTCCCGAGTGGGG[A/G]CGGGGCGGTGGCGAG | 79058 |
| rs536790120 | snp | A/G | 1.74048e-05 | 0.00294993 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996492 | AGCGTCGGCTGGCCA[A/G]GCAGCCGCCAGCGCT | 79058 |
| rs536797350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991786 | AGCCACAGCTTCTGT[C/T]CCCGGCAGGGCGCAT | 79058 |
| rs536815334 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003511 | GCCATGTGGCCACTC[A/G]CTGGCAGGCCCGGGC | 79058 |
| rs536825052 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994211 | CAGCTGTGCCTCCTG[A/C]GGGGCGAGGCTCAGA | 79058 |
| rs536859881 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995918 | TGGTCCTGGTGGTGC[C/T]GGTGCCCGGAGGGCT | 79058 |
| rs536874411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997122 | CTCCGGGATGAGGCC[A/G]TGTGGGCTCCGGGAT | 79058 |
| rs536954784 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011118 | CCTGAGTGCTCACGT[C/T]GCCCACCTACTGGGC | 79058 |
| rs536980449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987796 | AGGTTGCAGTGAGCC[A/G]AGATCGCACCATTGC | 79058 |
| rs537012815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007478 | GCCTGGGGGTCCTTG[C/G]CACTGTCCAGTATGC | 79058 |
| rs537105425 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985740 | TGGCACTTTGCAGTC[C/T]TTTGTAGAGGAGGGG | 79058 |
| rs537106310 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978989 | TGGTGAAGAAGGGAG[C/G]GAGAGTGGACAGGAT | 79058 |
| rs537281859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016403 | GGGGCCTGGCCCTGG[A/G]GGTGTAGCTGCCTTC | 79058 |
| rs537322618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987390 | AGAAAACCAAACAGC[A/G]CGGGGAACAGAAGTC | 79058 |
| rs537343774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006812 | CACCTGGCGCGGGAG[C/T]GGCGCTGATGCCACA | 79058 |
| rs537392331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983097 | TGATCCGCCTGCCTC[A/G]GCCTCCGAAAGTGCT | 79058 |
| rs537422323 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014572 | GCCTTCCTCCCGGGC[A/G]CGGTGGTGCCGCCTC | 79058 |
| rs537429692 | snp | A/G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991798 | TGTTCCCGGCAGGGC[A/G/T]CATGCTGCTGCCTGG | 79058 |
| rs537449875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990735 | ACGGCCCTCCTGGAG[G/T]CACCCGGAGGAGGAA | 79058 |
| rs537485259 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014771 | ACGTGGGCCTCCTTT[C/T]GGAAGCTCTTCCTGG | 79058 |
| rs537511742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991100 | GCCGTGGGAACTCAC[A/G]CAGCAGCTGAGCCGC | 79058 |
| rs537546639 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010350 | CTGGCTGACACGGTG[A/T]AACCCCATCTCTACT | 79058 |
| rs537601611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006062 | GTGTGCATGTCCTTG[C/T]GTGTGCGTGTCCTTG | 79058 |
| rs537610625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010476 | GGAGCTTACAGTGAG[C/T]CGAGATCATGCCACT | 79058 |
| rs537632587 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981762 | CAACCTCTGCCTCCC[A/G]GGTTCAAGCGATTAT | 79058 |
| rs537811909 | snp | C/G | 0.404559 | 0.196498 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009734 | CTGAGCGGGCCCCCT[C/G]TGAGGTCTGTGGATG | 79058 |
| rs537823314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979446 | TCTTCCAGCTTCTCA[C/T]GGCTCCAAGCGTTCT | 79058 |
| rs537873514 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004763 | CCTCTGACTCTGCCC[A/T]GCAAGAGGGGCAGGG | 79058 |
| rs537897694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001074 | CCCCTGCTCACACCC[A/G]GCCCTCTGTGGCTGA | 79058 |
| rs537959243 | in-del | -/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977513 | CGGGGCGCCGTGGGT[-/G]GGGGAAAGGGCGGGG | 79058 |
| rs537961452 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982305 | ACCTGCCCGTGGTCT[C/G]TGTGGTGGTGTCTGG | 79058 |
| rs537990099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999026 | CCTTTGTCCCTGTCC[A/T]GACCCCGCATCAGAG | 79058 |
| rs537994530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993509 | TGAGCCACCGCGCCC[A/G]GCTGAGTCCTGCTCT | 79058 |
| rs538055655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993913 | CTTTGCCTAGGCTCT[A/G]GCCATCTGCCCCCTC | 79058 |
| rs538074987 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014933 | CTTCTCCCTGTCAGC[C/T]GAGGGAGCCAGGCAG | 79058 |
| rs538125309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989561 | TAGGCGCTGTGCTTC[C/G]AAGGGGCGTTCTGAG | 79058 |
| rs538128259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000440 | GCGTCCTGCCTGCCC[C/T]GCGCCTCCCATCGCC | 79058 |
| rs538200830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985018 | CACACCTGCACACAC[C/T]GCCCACACCAACATG | 79058 |
| rs538315460 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005200 | GGGGCAGTCCTGGCC[C/T]GCTGGGCAGAGCAGA | 79058 |
| rs538438229 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983865 | TGAGCATCTCATGTT[C/T]TTTTTTTTTTGAGCT | 79058 |
| rs538516472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978104 | CCCATTCCGGGGCGT[C/T]CCCCGGAGCGGGAGC | 79058 |
| rs538555412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978726 | CCCGCAGAGGCTGCG[C/T]GGGACCCCTTGGTGC | 79058 |
| rs538560169 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989980 | TTTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 79058 |
| rs538587296 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976807 | TAAGCACATTCGACG[G/T]CTGCGAGTCAGGAGG | 79058 |
| rs538597028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005271 | GCGGAAACATGAGGC[C/T]GCGTGAAGTGGGCAT | 79058 |
| rs538605448 | in-del | -/AGCCCGTGGACCGGG | 0.00842714 | 0.0643627 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:82009035 | GCGCCCTCTGCCTCC[-/AGCCCGTGGACCGGG]AGCCCGTGGACCGGG | 79058 |
| rs538644932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997576 | CACTGCAGCCTCTGC[C/G]ACCCAAGTTCAAGTG | 79058 |
| rs538646665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987318 | TGGGTGAGAAGCAGG[A/G]ATCCCGGCGCCCTGG | 79058 |
| rs538703892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993083 | AACAAAAGAAAACAC[A/G]TCAAACCCACACACG | 79058 |
| rs538723932 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011487 | CCCAGGTGCTGGGGC[A/C]GCCCGGGGCTGGCGT | 79058 |
| rs538799604 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012495 | CTTCCTGCCTGGCCC[C/G]GGGTGGGAAAGGACC | 79058 |
| rs538829216 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002739 | TTTTTGTATTTTTAG[-/T]TAGAGATGGGGTTTT | 79058 |
| rs538870120 | snp | A/G | 0.0020496 | 0.0319468 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013479 | GGTGTCCCCGGTGAC[A/G]TGCCTGCCTGCCTGC | 79058 |
| rs538873593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008600 | GTTCCCTGGGGGCAG[A/G]CGTGCATGGATTCAG | 79058 |
| rs538896678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984193 | TTTTTCTTTCTTTCT[A/G]GGGTCAGTTGTGCCT | 79058 |
| rs538922056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009244 | CAGGGTTTGCCCCAT[C/T]GGGTGCTTGTGCTGC | 79058 |
| rs539018893 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982329 | TGTCTGGTGGGAACC[A/G]GTGAGTGCGATTTTG | 79058 |
| rs539084230 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010375 | TCTACTAAAAATACA[A/C]AAAATTAGTCAGGAG | 79058 |
| rs539136540 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007375 | AGTTTTGTTTTCCAA[A/G]TGAAGTCAACAGCCC | 79058 |
| rs539145905 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976521 | GACAGGAAGGCACAA[C/T]AGCACCCATGCAGAG | 79058 |
| rs539187948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995583 | ACGTGGCCAGCCAGG[C/T]CCGATCCCTGCCCAC | 79058 |
| rs539197568 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985374 | GAGGGTAGCCTTCTC[C/T]GTGGGGGTCAGCCTC | 79058 |
| rs539233585 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976977 | GGGTCGGCAGGAGCT[C/T]CGGTGAGACTCAAGT | 79058 |
| rs539253212 | snp | A/G/T | 0.000236703 | 0.0108767 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996046 | TCGCTGGGCCTGACC[A/G/T]GGGGCAGCGCCACCA | 79058 |
| rs539369758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011000 | TGGGTGGGTGCGGGT[A/G]CTGATGTCCCCTTGG | 79058 |
| rs539378455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992013 | TCTGCCCTCCTGGCC[A/G]TCCCGCTGGCTTCTG | 79058 |
| rs539381502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997067 | AAAGTAGCTTTACTG[A/C]GACGGTGGCTGTGTC | 79058 |
| rs539383731 | snp | A/C | | | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009289 | GCCAGCACTGGCTCC[A/C]GGCCCAGGTCCCTGA | 79058 |
| rs539434848 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993508 | GTGAGCCACCGCGCC[A/C]GGCTGAGTCCTGCTC | 79058 |
| rs539451867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994533 | TGCCGGCAGCTCCAC[A/G]TCCTGCCAGCGGCCC | 79058 |
| rs539598331 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987572 | AAATGGCCCAGAGTG[G/T]CCTGGGGCTGCCACT | 79058 |
| rs539631246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985670 | AAGCTGCTGTGGTTA[C/G]TGGGTCTGGTTCAGA | 79058 |
| rs539659449 | in-del | -/TGGGAAGGTGACCGCGCGTCGGGCGC | 0.204496 | 0.245824 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986725 | CGAGCATAGGGCCTG[-/TGGGAAGGTGACCGCGCGTCGGGCGC]TGGGAAGGTGACCGC | 79058 |
| rs539685772 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991724 | GCTGTCATGTGGTGG[A/G]TGATGCCCTCTGCGG | 79058 |
| rs539716218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980996 | ATAGTGAGACCCTGT[A/C]TCTACAAAAAAAGTA | 79058 |
| rs539718173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986314 | GTGCGTGCCTGTGGT[C/T]CCAGCTATGCCAGAG | 79058 |
| rs539733694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010647 | GCCCAGCCTGCCACG[A/G]GGGAGTCAAAGCCCA | 79058 |
| rs539811875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013606 | GGCAGAGCCCCACTC[C/T]GGCTGCCTGCTGCCT | 79058 |
| rs539832028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978374 | AAAAAAATACAAAAA[A/G]ATTTAGCCGGGCGTG | 79058 |
| rs539842304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000332 | GGTGGGGTCTTGGCT[A/G]GCAGGAGGGGTCCAG | 79058 |
| rs539949931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990660 | GGGAGTGTGCCTTCC[A/G]TGATAGGAGACGCAT | 79058 |
| rs540124112 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015773 | GGCGCTGTCCTCCCC[C/G]TGCCCCCTTCCTGGC | 79058 |
| rs540135094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993644 | CTGTCCCAGCATCCC[A/G]CTCTGTGCATGGATG | 79058 |
| rs540191611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002994 | ATTTTCGTGTCTCAG[C/T]CTCCTGAATAGCTGG | 79058 |
| rs540200918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989330 | GGCGTTGCCAGCCCC[A/C]CGGTGAGGGTGGAGT | 79058 |
| rs540248454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014212 | CCCCTAGCCAGTTCT[A/G]TCGTCCTTCCTTTCC | 79058 |
| rs540305430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978869 | TAAGGCAGGTTGCAG[A/G]ACTACAGGGTTTGAA | 79058 |
| rs540312084 | snp | C/T | 0.429837 | 0.173662 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009791 | TCTGAGGGGGCCCCC[C/T]GTGAGGTCTGTGGAT | 79058 |
| rs540321857 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004277 | AGGGCTGCCCCCGGC[A/G]TCCCGGACAGCGTCC | 79058 |
| rs540410787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992815 | GGCTGCTCTGTGGGA[C/T]GGGAGCTTAGGGAGT | 79058 |
| rs540419936 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986951 | GGCCCCTGGAGATGG[-/C]CAGCGGGTTAAGCAC | 79058 |
| rs540451805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998652 | ATCAATGGAGATGAC[C/T]GTATGCTTTATTTTA | 79058 |
| rs540525795 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017831 | GATGACTTCTACAGG[C/T]TCCCAGGGCTTTCAA | 79058 |
| rs540671274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991820 | GCTGCCTGGGCTCTC[A/G]TCAGCACCTGTGTTT | 79058 |
| rs540686568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987047 | AAAGCCACGGGCAGG[A/G]GTGAGCGGGACCCGA | 79058 |
| rs540752440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987447 | TGCCCCTGGGCCGGG[C/T]GGTGCCCCCGGGCGT | 79058 |
| rs540776974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982431 | CAAAGTGCAGCCGGT[A/G]CAGAGGAATGCAGCC | 79058 |
| rs540784253 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988829 | AGCAGAGTGTGCAGC[G/T]GGAGGCCTTTGCACC | 79058 |
| rs540813923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983116 | TCCGAAAGTGCTGGG[A/G]TTACAGGCGTGAGCC | 79058 |
| rs540824834 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993236 | TGTTTGTGTTTGAGA[C/T]GGAGTCTCGCTCTGT | 79058 |
| rs540832509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988223 | TCCAACCCTTTGGGA[G/T]GCCGAGGTGGGTGGA | 79058 |
| rs540833554 | snp | C/T | 5.04723e-05 | 0.00502331 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016959 | CATGTCCAGGGCCGC[C/T]GGGTCCCCTTCCCCA | 79058 |
| rs540853879 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977995 | TGAGGTAGAACGGCG[C/T]CGCGTGTCACCCGCA | 79058 |
| rs540887976 | snp | A/G | 1.97689e-05 | 0.00314389 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983651 | GCTTCCCGGAGCCGT[A/G]AGGGGCCTGAGAACA | 79058 |
| rs540893799 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988565 | CCCCCAGCCTGCGGC[C/G]CTGGTCTGTGTGGCA | 79058 |
| rs540894901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012358 | GAGCGTGAGGCCTCG[G/T]GCAGGAAGGAGGGGC | 79058 |
| rs540941971 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976590 | CTCACGTGTGTAATC[A/C]CAGCCCTGTGGGAGG | 79058 |
| rs540975553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983943 | GCTCACTTCAAGCTC[C/T]GCCTCCCGGGTTCAC | 79058 |
| rs541097378 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015849 | CCCACCCCACAGGCC[C/T]TTCTCTGCTCACAAG | 79058 |
| rs541117612 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981967 | CACTGCACCTGGCCT[C/T]ATTTTTCTTTCTTTT | 79058 |
| rs541123468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016556 | GTTGGGGCCAGTGTC[A/G]GAGTCCAGCCAGCCT | 79058 |
| rs541182784 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011963 | CTCCCTTGGAGGGTG[G/T]CTAGGTGGCAAAGGG | 79058 |
| rs541377805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005429 | GGCCTCATCTGAGAC[A/G]GGAAGCCCCACGCAG | 79058 |
| rs541384405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015477 | CCTGCCCGCCCCTTT[C/T]TGTGCGTCCCGTGGG | 79058 |
| rs541401318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996327 | GGCGGGAGAGGGTGA[A/G]CCGGGGGCGGGAGAG | 79058 |
| rs541429496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981197 | GTCAGATACCAGCCC[A/G]GGGGTCTTTGGAAAG | 79058 |
| rs541445999 | snp | C/T | 4.99904e-05 | 0.00499927 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010765 | TCCCTGGTGCAGCTC[C/T]GGCCGTCCCTCCAAC | 79058 |
| rs541476860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999514 | TGCCTGTAATCCCAG[C/G]TACTCGGGAGACTGA | 79058 |
| rs541526414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006471 | CACTGTTGTGTCTGC[C/T]CATCTTTCTGTGGGC | 79058 |
| rs541536232 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994189 | CCTGCCCACCCATGC[A/C]CGGGTCCAGCTGTGC | 79058 |
| rs541589920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007069 | AGTGACATTTCCCAG[C/T]AGCCCTACTGCAGAC | 79058 |
| rs541657022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001283 | GGCCAGGGGCTCCTG[C/T]CCCTGGACCCTGACG | 79058 |
| rs541749394 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991467 | AGGACAGGGCTCTGC[A/C]AGGTGGAGCACTGGC | 79058 |
| rs541760369 | snp | A/G/T | 0.00039621 | 0.0140697 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015127 | GTCCCTCGCTGAAAC[A/G/T]GTGCCTGGGACCAGA | 79058 |
| rs541817336 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987887 | CAACAAGGCTGGGCA[C/T]GGTGGCTCACACCTG | 79058 |
| rs541856848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006086 | GTCCTTGCGTGTGCA[C/T]GTGTGTGCTTGGGGG | 79058 |
| rs541967579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989681 | GGATGGACACTGCCA[C/T]GTGTTTGAAACGTTG | 79058 |
| rs541985330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984494 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 79058 |
| rs542026413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014334 | CTACCCCACCTGGAC[C/T]CTCTGAAATGTTCCT | 79058 |
| rs542032933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985051 | CACACCTCCCCCCCA[C/T]ACACACCCACGCACA | 79058 |
| rs542034904 | snp | C/T | 0.000123816 | 0.00786719 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009533 | AGGCCTTCAGGGAGG[C/T]GCAGATAAAGGAGAA | 79058 |
| rs542046352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990342 | TGCTGCAGGGAGGGC[A/G]TCAGGAGACAGAGGC | 79058 |
| rs542049192 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009984 | GTGCCATCTCAGCTC[A/G]CTGCAAGCTCCGCCT | 79058 |
| rs542071142 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978998 | AGGGAGGGAGAGTGG[A/C]CAGGATTTGCAGGTG | 79058 |
| rs542107735 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985434 | CTCTCTGTGTCTGGA[C/G]AATCAGTCTGGGATT | 79058 |
| rs542108721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010296 | GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAT | 79058 |
| rs542132203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990801 | TACAGATTGTTATGC[C/T]AACGGGTTTCCTATG | 79058 |
| rs542166516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998456 | TGGTGCTTTTGGATC[A/G]TGGCGATCTTAGTAG | 79058 |
| rs542187501 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012519 | AAGGACCTGCTAGGC[A/G]GCCTGCCTGAACTGA | 79058 |
| rs542204616 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983910 | TCGCCCAGGCTGGAG[C/T]TCAGTGGCGCAGTCT | 79058 |
| rs542227058 | snp | A/C/T | 0.00163958 | 0.0285876 | downstream-variant-500B, intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017443 | CCAGAAAAGGGCCCC[A/C/T]GTCGTCTGCCCTGGC | 79058 |
| rs542232896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993535 | GCTCTTTCAAGTAGG[C/T]CAGCAGATCCCAGGG | 79058 |
| rs542273969 | snp | A/G | 1.80354e-05 | 0.00300289 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983587 | CGACCTTTCTCTCCA[A/G]TGGAGATTTGCCAAC | 79058 |
| rs542310829 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977547 | GGCAGGACCCGGAAG[C/T]GCGCTGCGGCCCCGC | 79058 |
| rs542418746 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981816 | TGGAATTACAGGCAC[A/G]TGCCACGCCTGGCTA | 79058 |
| rs542437267 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014582 | CGGGCACGGTGGTGC[C/T]GCCTCCCTCCCAGGC | 79058 |
| rs542556582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998082 | TCCGCCCGCCTCAGC[C/G]TCCCAAAGTGCTGGG | 79058 |
| rs542645484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008391 | CTGTGTGAGGGGGGA[C/T]GGGGCCGAGTGTGGG | 79058 |
| rs542673900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012883 | CGCCCTCCAGAGCCA[A/G]AAGCAATGAATGTCC | 79058 |
| rs542715646 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013561 | AGGCAAGCAGGCGGC[A/G]GGCGCGGAAGCACCA | 79058 |
| rs542748628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978214 | GGGCACCTTGTGACC[A/G]CGAATCAATTAAATG | 79058 |
| rs542760509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003722 | GCGTCCTTTGTGCAT[G/T]CCTGTCCACGCCGGT | 79058 |
| rs542815063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009334 | CAGGACCTCAGAGGG[C/T]TGGGGCCCAGGGAGG | 79058 |
| rs543008417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001191 | GGGTCATGCACTGGG[C/T]GTGGTGAATACACCC | 79058 |
| rs543034230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995630 | GGAATGGCCACCCCC[A/G]TGGGTGACAGCACGT | 79058 |
| rs543036231 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990912 | CGTCTGGGCAGTCCA[C/G/T]GAGGGCAGGCGGGCG | 79058 |
| rs543042974 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001983 | GTTCTTATTTTTCTT[C/T]TCTTTTTTTTTTCTT | 79058 |
| rs543097423 | snp | A/C/G | 0.00159649 | 0.0282165 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991394 | CGTGGCTCCGGGAAA[A/C/G]CTGGGTGATTTCTGC | 79058 |
| rs543104283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996357 | GGGTGAGCCTGGGCC[A/G]GGAGAGGGTGAGCCG | 79058 |
| rs543259122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011375 | CAAGTGTGGCCCGCA[C/T]GGTGGCCCAGCCACG | 79058 |
| rs543268283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987012 | CTCAGACAACAGTGA[C/T]GGAGCCTAAGAGCAA | 79058 |
| rs543305086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982366 | GTCCTGCAATACCAT[A/G]GCCATGTTTTCAGGT | 79058 |
| rs543321809 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011804 | CCCGAGCCAGGCGGT[G/T]GGAGCCAGGCTTCCT | 79058 |
| rs543329022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992685 | CTCTCTGCCTCTGTC[C/T]GGGTTCTGCTCCGGC | 79058 |
| rs543365442 | in-del | -/GT | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990973 | GGACCTAGTTGCCAA[-/GT]GTGGTGAAAGGCAGG | 79058 |
| rs543389844 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988062 | ACTCAGGAGGCTGAG[A/G]CAGAAGAATTGCTTG | 79058 |
| rs543410255 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004030 | AAACCCTCAGAGACG[C/T]TGGAAACTCTGAGGT | 79058 |
| rs543428266 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990704 | GGATTTCATGGCCTA[C/T]GGGCCCTGGGGGTAC | 79058 |
| rs543448779 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006017 | ACAGTCTGTGGTTTT[C/G]TTTTGTGTGCATGTC | 79058 |
| rs543448826 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978120 | CCCCGGAGCGGGAGC[C/T]CGGGTTGCGCGGTGG | 79058 |
| rs543620448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982056 | ACACTGCAACCTCCG[C/T]CTCCCGGGTTGAAGC | 79058 |
| rs543783077 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976107 | GCCTTAATTACTCCA[C/G]AAGGAGCCACGGACC | 79058 |
| rs543816945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985379 | TAGCCTTCTCCGTGG[A/G]GGTCAGCCTCTCCCT | 79058 |
| rs543837623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009819 | GATGGGACGTGGGGG[C/T]GACTGAGGCACAGCT | 79058 |
| rs543842368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010267 | GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 79058 |
| rs543898929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005008 | TCTGGGCCTCTTTGC[A/G]TCGGCTCAGGGGAGG | 79058 |
| rs543909174 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015557 | GTGCCTCTCTGCATC[A/G]GTGGCCTCTGAGGGA | 79058 |
| rs543940770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010382 | AAAATACAAAAAATT[A/G]GTCAGGAGAGGTGGC | 79058 |
| rs544000952 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010727 | TGGCCCAGCATGGGC[C/T]GAGTGGGGAGGCCAC | 79058 |
| rs544160036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997314 | AAGGGGTGGGGCATT[C/T]AGAAATCTCTAGAAA | 79058 |
| rs544161417 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989851 | GGAGTGCAGTGGTGC[A/G]ATCTTGGCTCACTGC | 79058 |
| rs544163418 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015702 | TGAATCTTGGAGGCC[C/T]GGTGGTGGCGGAGCA | 79058 |
| rs544218959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992862 | GCAGAGGACACCCGC[C/T]GTGTGTGTGGTGCGC | 79058 |
| rs544319290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998856 | CCCACCACTGGGGCA[C/G]TGGGCCCTTGGCGGG | 79058 |
| rs544327239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992082 | TGTGAGAGTGTGCCA[G/T]TACCCTGCTGCGAGC | 79058 |
| rs544383615 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017907 | CAGCCCTGCCTGCCC[A/G]GGGCCACTGGGGCTA | 79058 |
| rs544405270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986635 | GAGCCAGGGGGTTCT[C/T]GCCCTCCCCGGGCCT | 79058 |
| rs544448913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013663 | GCTTCCGAGAGGGAC[A/G]GCGTGCGTGGGTGTG | 79058 |
| rs544501822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994552 | TGCCAGCGGCCCCGA[G/T]ACTGGAGGTCTCGGG | 79058 |
| rs544514613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014256 | CCGTCCTGCACTGCC[A/G]TGTCGCCCACTGCCG | 79058 |
| rs544552457 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004182 | CTCACCCTGCAGCCC[C/T]CAGCCTCCCTCCCCT | 79058 |
| rs544562851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990274 | ACTTGGAGCATCTCG[C/G]TCTGGGCCGGGTCCT | 79058 |
| rs544749760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983478 | GCGTGGATGGTGGGA[C/T]GGGGATGGCGGGGCG | 79058 |
| rs544787048 | snp | C/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977453 | AGGCAGAGGACGACC[C/G]CGCTTTCCGGGTCTG | 79058 |
| rs544797022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989192 | CAGCCTGGGCGACAG[A/G]GCAAGACTCTGTCTC | 79058 |
| rs544846050 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984433 | AATACAAAAATTAGC[C/T]GTGGGTGGTGGCGGA | 79058 |
| rs544875176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978562 | TTATTGAGCCTCTGC[C/T]GCGTGGGGGACCGTG | 79058 |
| rs544911390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008957 | AGTCTGTGTGACCAC[C/T]TCGGCTGGGGCACTG | 79058 |
| rs544966137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978914 | GTGTGCCAGGAAGAT[A/G]CCCGTGTTGCTGTAC | 79058 |
| rs545134768 | snp | A/G | 0.000141004 | 0.00839536 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017384 | CCTCTGCCAGCAGGA[A/G]TAAAGACTTGTGCAT | 79058 |
| rs545136983 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012425 | GAGCCGGTGGGTTCC[G/T]AGGGGGCCGTGCGCC | 79058 |
| rs545347554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000106 | GCTCCGGGTGAGCAG[A/G]GGCTGACCCCCTCTA | 79058 |
| rs545359301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011303 | TAGGCTGGGGCGGGG[A/G]TGGGGCTGGGGGGCA | 79058 |
| rs545387367 | in-del | -/GGGGCAAGGGGTTGGCAGCAGAGAGGC | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014798 | CTGGCAACACTGAGT[-/GGGGCAAGGGGTTGGCAGCAGAGAGGC]GGCTGGATTTGGGGC | 79058 |
| rs545413638 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994637 | GTCAGGTGCCTCCTT[C/T]TGGTGGTTGTGGGGC | 79058 |
| rs545420289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992226 | GGACATTGGGACTTG[C/T]AGAGGTCTGCGTGGG | 79058 |
| rs545423132 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994461 | CTGAGTACAGGTGTC[C/T]GTGAGCCGCATTCCG | 79058 |
| rs545437147 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006302 | GTGCGTGTTTGGGGG[G/T]GTGTGTGTGTCCTTG | 79058 |
| rs545445267 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981178 | TGGCGGGAGGTTGGC[A/T]GATGTCAGATACCAG | 79058 |
| rs545488815 | snp | C/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975927 | AAGGGGAAGCTTGAC[C/T]GAAAGTGACTATAAA | 79058 |
| rs545552069 | snp | C/T | 0.000110994 | 0.0074488 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015049 | CTCTGGCTGGGGGGA[C/T]GGTGTGACCCACTTT | 79058 |
| rs545638018 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996349 | GCGGGAGAGGGTGAG[C/T]CTGGGCCGGGAGAGG | 79058 |
| rs545639755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015584 | GGGAGCCCTCTCGCC[C/T]GGCAGCAGGTGGGAT | 79058 |
| rs545650274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985988 | CTTTTTTTTAAGAGG[C/T]AGGGTCTCACTATGT | 79058 |
| rs545663376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991901 | ACTCACTGCCTTGTC[C/T]CCAGCACACAGCCGC | 79058 |
| rs545684097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991321 | CTCCCAGCCTTGACT[C/T]AGTGCTTGGGGGCTG | 79058 |
| rs545702824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015984 | GGCCTTTGAAGCTTC[C/T]TCTTATTAATCTTTT | 79058 |
| rs545716070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987098 | AAGAGCAAAGCGAAG[A/C]CACGGGCAGGGGTGA | 79058 |
| rs545737405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986589 | AAAAGGCTCAGCAGA[A/G]TGGAAGGGACTTGGG | 79058 |
| rs545803667 | in-del | -/A | 0.166832 | 0.235761 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978526 | GCGAGACTCCATATC[-/A]AAAAAAAAAAAAAAA | 79058 |
| rs545852559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985095 | ACACCTACACATCTG[C/T]GCACATACCCGCACA | 79058 |
| rs545926724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990895 | CGGGGGATACTGTAG[C/T]ACGTCTGGGCAGTCC | 79058 |
| rs546052217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010306 | AGGCCAAGGTGGGCG[A/G]ATCATGAGGTCAGGA | 79058 |
| rs546166014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982031 | TGGAGTGCAATGGCG[C/T]GATCTTGGCACACTG | 79058 |
| rs546182001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989727 | GGTGTCACTGTAGCA[C/T]GCAGCCCTGGCCCGA | 79058 |
| rs546205754 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006255 | TGCATGTGCATGCTT[-/G]GGGGGGCGTGTGCGT | 79058 |
| rs546301412 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003549 | ATCGGTGCGGATGCT[A/G]TGCTCAGCCTGGGGG | 79058 |
| rs546329713 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014619 | GTGCCGCCTCCCTCC[C/T]GGGCGTCTTGAGCTG | 79058 |
| rs546465168 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004260 | TGAGGCCGCGCGCCC[A/G]CAGGGCTGCCCCCGG | 79058 |
| rs546467493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006095 | TGTGCACGTGTGTGC[C/T]TGGGGGCGTGTGTGT | 79058 |
| rs546509917 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998001 | CCAGCTAATTTTTGT[A/C]TTTTTAGTAGAGACG | 79058 |
| rs546575648 | in-del | -/TG | 0.0146672 | 0.084371 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009649 | ACGGGATGGGGCGAC[-/TG]AGGCACAGCTCTGAG | 79058 |
| rs546632703 | snp | A/G | 1.75145e-05 | 0.00295921 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996445 | AAGTGCTACGACCCC[A/G]TGGGCAAGACCCCAG | 79058 |
| rs546650705 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982556 | TGTGGCAATTTCCAG[A/C]CTCACTTTTCTGGCC | 79058 |
| rs546767683 | snp | G/T | 2.34767e-05 | 0.00342604 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017128 | GGTACTGCGGCTGGG[G/T]GGAAGGTGGGGTGCT | 79058 |
| rs546770586 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998118 | AGGCTTGAGCCACCG[C/T]GCCCAGCCTAATTTA | 79058 |
| rs546789388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993362 | GGGACCACAGGCGCC[C/T]GCCACCACGCCTGGC | 79058 |
| rs546867098 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977149 | GTCCCAACACCCAGG[C/G]AGGATCCGTACAGGG | 79058 |
| rs546918460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012472 | ACACGGCTTTCCGGC[C/T]TCCTCTGCTTCCTGC | 79058 |
| rs546924346 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010196 | CAAAGTTCTGGGATT[A/T]CAGGCTTGAGCCACC | 79058 |
| rs546939026 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976957 | GGAAGTCCTTGAGTG[C/T]CTGTGGGTCGGCAGG | 79058 |
| rs546980198 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008567 | CATCCCAGGGTGGGC[A/G]GAGGGAGGGGCCGGC | 79058 |
| rs546983703 | in-del | -/CACACACCCGCACACACCC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984940 | ACACCCCCACACCCG[-/CACACACCCGCACACACCC]CACACACCTGCACAC | 79058 |
| rs547049596 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999360 | CCTGTGGCATGGTGG[C/T]TCACACCTGTAATCC | 79058 |
| rs547094031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006729 | CAGGGCCCTCGCTGT[C/T]GCTTTTTTCCCTCAC | 79058 |
| rs547095245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987263 | AGCCAGGAGTGGCGC[C/T]GGGCAGGGAGGCAGG | 79058 |
| rs547114933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016175 | CCTTCCTCGGGTGCA[A/G]AGGCCAGAGGAGGGA | 79058 |
| rs547150484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982681 | GCATTTCCAAAGTGA[A/G]GCCAACCACTTTGAG | 79058 |
| rs547156688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987668 | GACTTTGTAAACCTC[A/G]TGTGAAACTTAGTTT | 79058 |
| rs547157233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007316 | GGCCCTTGGGATGAC[A/G]GGTAGGAATCTAGGG | 79058 |
| rs547220508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001592 | GAACCCCGGGGGGTA[C/G]GGGGTGGATGCTCGC | 79058 |
| rs547223504 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975572 | CCTACCTCAGTGTCC[C/T]GAATAGCTGGGATTA | 79058 |
| rs547273726 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013084 | GCCTGGGGCTGCAGC[C/T]GCTTACTGAGCTGGG | 79058 |
| rs547347412 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015757 | GACCATGGCAGCTCC[G/T]GGCGCTGTCCTCCCC | 79058 |
| rs547391832 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981523 | AGCTGGGATTACAGG[C/T]GTGCGCCATCATGCC | 79058 |
| rs547408311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010973 | CCACCTGGCCTGCGG[A/G]CTCCAGGGCACTGGG | 79058 |
| rs547437814 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010400 | CAGGAGAGGTGGCGC[A/G]CGCCTGTAGTCCCAG | 79058 |
| rs547504557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999822 | TCCCGGCCACACACC[C/T]GGGAGGGCAGAGGCC | 79058 |
| rs547600313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990585 | TCCACGCCGAGCTCT[A/G]GGGGACACTGCTCTC | 79058 |
| rs547663054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990934 | AGGCGGGCGAGTCCC[A/G]TAGTTTGAATCCCAC | 79058 |
| rs547688647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995333 | GGCCAGGACATTCCC[C/T]GCATTTATCCCCATT | 79058 |
| rs547793583 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982149 | AATTTTTGTATTTTT[A/G]GTAGAGACGGAGTTT | 79058 |
| rs547842282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006119 | TGTGTGTGTCCTTGC[A/G]GGTACACATGCGTGC | 79058 |
| rs547857959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000295 | TGCCCGCCCGTGCTC[A/G]CCCGTCGGGAGGCGC | 79058 |
| rs547962279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000943 | GCTGGCACGAGGGCC[A/G]CTCCTGATCAAAGGC | 79058 |
| rs548055369 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014539 | GGTGCCATCTCCCTG[C/T]CGAGGCACTGTGGTG | 79058 |
| rs548110132 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979198 | GGTTCTGGAGGACAC[A/G]TGCCGGCGGCAGGAC | 79058 |
| rs548190136 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984883 | ACCCCCGCACACACA[-/C]CCCCCACACACACCC | 79058 |
| rs548266470 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017581 | CTTCGTTTTTAACCT[A/G]ACAGTTATTTACACT | 79058 |
| rs548281709 | snp | A/G | 6.86648e-05 | 0.00585898 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009154 | GAGCTGACGGTGGAC[A/G]ACGTGAGAAGACGCT | 79058 |
| rs548283879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989470 | GGAAGTCCAGGTGTC[C/T]GCAGAGTGGGACGGG | 79058 |
| rs548317147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983738 | GCCAGGGACGGGGGA[C/T]GGGACAGTGGGGGGT | 79058 |
| rs548336533 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013341 | GCAGCCCACCCTCCC[A/G]CTGGGAGGCCCCTGA | 79058 |
| rs548343693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009636 | GTGAGGTCTGTGGAC[A/G]GGATGGGGCGACTGA | 79058 |
| rs548382180 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978062 | GGGCGCCGGGAAGAG[A/G]GAGGAGTGGAGCCCT | 79058 |
| rs548399172 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004598 | CTCCACGCTCCTTGC[C/G]TCCTTGTGTGTCATG | 79058 |
| rs548461901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005043 | CCGTGGCTGGGCGAG[A/G]GTCAGCTGCCATTTG | 79058 |
| rs548540089 | snp | A/G | | | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017913 | TGCCTGCCCGGGGCC[A/G]CTGGGGCTACATCGA | 79058 |
| rs548589437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998180 | CTCTCTCTGTTGCCC[A/G]GGCTGGTCTCGAATT | 79058 |
| rs548634679 | in-del | -/GT/GTGT | 0.0977899 | 0.200675 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006213 | TGCATGTGCACAGGT[-/GT/GTGT]GTGTGTGTGTGTGTG | 79058 |
| rs548651771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984017 | CCGCCACCACACCCG[C/G]CTAATTTTTGTATTT | 79058 |
| rs548700010 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993130 | TGTCGGGGCTGGGCC[C/T]GTCCTGGGTGTGGCA | 79058 |
| rs548780624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992489 | AGCTGGCGGTCAGTG[C/T]CGGGGAAGGACTGTG | 79058 |
| rs548793936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003165 | AAATAACTTTTCTTG[G/T]CTGGGTACAGTGGCT | 79058 |
| rs548841432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987801 | GCAGTGAGCCGAGAT[C/G]GCACCATTGCACTCT | 79058 |
| rs548841582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993039 | TGCCCCTCCCCCAGG[A/C]TTGAGGACGTGAAAA | 79058 |
| rs548927733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999158 | GGGGGACTGTCATGC[A/G]GCTTTCGGTGACAGG | 79058 |
| rs548965999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012440 | GAGGGGGCCGTGCGC[C/T]TCTGAAGTTGCTTCT | 79058 |
| rs548966341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008189 | ATGGTGGGGGTGCTG[A/G]AATGCTGTGTAGGGC | 79058 |
| rs548977698 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976859 | GAGCTGGTGAGGCCA[A/G]GTGCTTTCCCTGCTG | 79058 |
| rs548989350 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980549 | TTGTCAACTGAAGAA[C/T]GCGGTTCATATGTTT | 79058 |
| rs549081566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001559 | CTGGTGACTGACAGG[C/T]GCTTGTGTTTTGGTG | 79058 |
| rs549439011 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976342 | TAAAACCCACCAGGT[G/T]ATGTGTGGCTCAGTA | 79058 |
| rs549470868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010481 | TTACAGTGAGCCGAG[A/G]TCATGCCACTGCACT | 79058 |
| rs549498711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991569 | CATCCCTGCCCGTCC[C/T]TGTTCATCCCTGTCC | 79058 |
| rs549517848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986851 | CACGGGTGTTGCGTT[C/T]GTGGGTGAGAGCGCT | 79058 |
| rs549530603 | snp | C/T | 3.38278e-05 | 0.00411251 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010891 | GCGCTGTGGGGTGTC[C/T]GGGGATGGGGGGCAG | 79058 |
| rs549561838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991930 | GCGCCTTGCCGGAGC[A/G]GGGCCCCAGCGGGGC | 79058 |
| rs549614830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015669 | CCTGGGCTTCTGTGA[A/G]CAGCCGCAGCCTGGG | 79058 |
| rs549621582 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987171 | GAAGCCACGGGCAGG[G/T]GTGAGCGGGACCCGA | 79058 |
| rs549637285 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981460 | CTCGGCTCACTGCAA[A/C]CTCTGTCTCCCAGGT | 79058 |
| rs549704936 | snp | C/G | 2.66485e-05 | 0.00365015 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012128 | AGGGGCTCTTCTGCC[C/G]CACTTGAGGCGTCAC | 79058 |
| rs549752566 | snp | C/G | 3.31532e-05 | 0.0040713 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985538 | AGCTGGACGATGGCT[C/G]GAGGTTGCAGGACTC | 79058 |
| rs549771626 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975731 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC | 79058 |
| rs549778387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979829 | TACACGTACGCTTCT[A/G]TGTGGGGATATTGTT | 79058 |
| rs549838464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980812 | CTCTTCACGGGTCCT[A/G]TGTGCAAAAAATGGC | 79058 |
| rs549905053 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983002 | TGTATTTTTAGTAGA[A/G]ATGGGATATTTTTGT | 79058 |
| rs549954555 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005220 | GGCAGAGCAGAACAC[A/G]GCCTCTGCTCAGTGG | 79058 |
| rs549975583 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006599 | GGACGCCTCACCCCC[A/G]GTTGACGTCATTTTT | 79058 |
| rs549999060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994299 | GCAAGCGGGCGTGAG[C/T]GGAGTGCAGCGCCCC | 79058 |
| rs550039661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001037 | CTTGCTCCTGGAGCC[A/G]GGGCCTGGGGTTTCC | 79058 |
| rs550059650 | snp | A/T | 4.99713e-05 | 0.00499831 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994812 | ATGGTTTCTTTCCTC[A/T]CCTCCCAGGGAGTGC | 79058 |
| rs550082533 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978557 | AGTATTTATTGAGCC[-/T]CTGCTGCGTGGGGGA | 79058 |
| rs550183336 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014662 | TCTTGGCTTCGTTCC[C/T]CGGAGGGTGGTGCTG | 79058 |
| rs550258770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005676 | GTGGGGATGTTTGTA[A/G]GGACAGTGGTATGGC | 79058 |
| rs550504456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984199 | TTTCTTTCTGGGGTC[A/G]GTTGTGCCTTCCCTG | 79058 |
| rs550525233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001654 | GGGCTCCGTACTGGG[C/T]GAGTCGGCTGCTGCA | 79058 |
| rs550525753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004428 | GACCTGGGGGTCCAC[C/T]GGGGGCCTGGGTTTG | 79058 |
| rs550570172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997670 | ATTTTTTTGTATTTT[C/T]AGTAGAGACAGGGTT | 79058 |
| rs550618051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017225 | GTGGCCGGCAGGGCC[C/G]AGTGCTTCAGCCGGG | 79058 |
| rs550682656 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012496 | TTCCTGCCTGGCCCC[C/G]GGTGGGAAAGGACCT | 79058 |
| rs550682823 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017553 | GTGCATCCTGAACCC[A/G]CGTGGGTCTCCTCTT | 79058 |
| rs550693469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993375 | CCCGCCACCACGCCT[A/G]GCTAATTTTTTGTAT | 79058 |
| rs550719860 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987745 | TGGAGCTGGCTTTGG[G/T]GGTGGCTGTGGGGGT | 79058 |
| rs550744814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013210 | AGCCCCCGAGCTGCC[A/G]GGCGGACTCCGGGCC | 79058 |
| rs550754113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993720 | CCCTCCCAGTACCCC[C/G]CATCCCGGAGGGTTG | 79058 |
| rs550787693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983375 | AGGCCCCATATGATC[A/G]GGGACCCGCCTTGTG | 79058 |
| rs550842309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984688 | GGCTGCAGTCAGGTT[C/T]GGTGGAGCTGCAATC | 79058 |
| rs550884343 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987418 | GTCAGGAAAGATGAA[C/G]GTCTGGAAGGAAATG | 79058 |
| rs550915151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014514 | ATGCTGCCTCCCTCC[C/T]GGGCTCTGTGGTGCC | 79058 |
| rs550937454 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999162 | GACTGTCATGCGGCT[A/T]TCGGTGACAGGGATG | 79058 |
| rs550938532 | snp | A/G | 0.000324538 | 0.0127344 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009085 | GTGGTGTGCCACCCC[A/G]ACCTGGAGGAGCGGC | 79058 |
| rs550979879 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975627 | TAATTTTTGTACTTT[G/T]TTTTTAAGTAGAGAC | 79058 |
| rs550982125 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982526 | CTGCTATCCTGTCTT[A/G]ACGTAGACATTTCAT | 79058 |
| rs551036280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988322 | AAAAATTAGCTGGGC[A/G]CAATGGCTCATGCTT | 79058 |
| rs551083546 | snp | C/T | 5.69995e-05 | 0.00533821 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983698 | GGGGGAGGCTGACTG[C/T]GTGGGGCACAGGATC | 79058 |
| rs551200250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008092 | CAGTCGAGGTCTCAG[A/G]TGTGTCCGGAGGGCA | 79058 |
| rs551255736 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002328 | CAATGGCACGATCTC[A/G]GCTCACTGCAACCTT | 79058 |
| rs551256554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996923 | GTGGCTTTAGCTGGT[C/T]AGCCTGGTGGCGTGG | 79058 |
| rs551258410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992065 | CTGCTGGCTGGAGAG[A/T]GTGTGAGAGTGTGCC | 79058 |
| rs551263993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009430 | AGGAGCCCGGGGCCT[A/G]TTGCCAGGGCCCCCA | 79058 |
| rs551381852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016608 | CTGCCCGGGAGGGCG[C/T]TCGGTCTGGGGCCTC | 79058 |
| rs551400987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007400 | CAGCCCCCTAGCAGC[A/G]TGATGCTGATGGTCC | 79058 |
| rs551445050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012023 | CTGCACGGGTGGTGT[C/T]CCCTGCAGGTGGGCC | 79058 |
| rs551457619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006531 | GAAAGAGAAAGGAGG[A/G]TGCTTGTCTCTCTCC | 79058 |
| rs551687735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982215 | CTCAAGTGATCTGCC[C/T]GTCTGGGCCTCCCAA | 79058 |
| rs551701297 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991520 | TCTGTGCATGCTGCT[C/G]GGCCAGCTCAGAGCT | 79058 |
| rs551769512 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000354 | GGGGTCCAGGGGAGG[C/G]AGCGTGTGCCTGGCC | 79058 |
| rs551781129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986777 | ACTGTGCGTTGGGCG[C/T]GCTTGGTGGCCCCAG | 79058 |
| rs551833077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001001 | GCTGCCCTGCCTGCC[C/T]CTCCCGCCTCGGGGG | 79058 |
| rs551844111 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004970 | CTCCCATGGACCTGC[A/G]ACCTGCTGCCCGGGG | 79058 |
| rs551941100 | snp | A/G/T | 3.5872e-05 | 0.00423497 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015295 | CTCCACCATCCCCTC[A/G/T]TCCGAGCAGTGGCGA | 79058 |
| rs551956911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986355 | GAGGATCACTTGAGC[C/T]GTGGAGGCAGTTGCA | 79058 |
| rs551962114 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995835 | CTGGGCCTTGTGGAG[A/G]GTGTGGACCGGCAGG | 79058 |
| rs551966654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990422 | TCTGCCCAGCACAGA[A/G]GGGTGTGAACAGCCA | 79058 |
| rs551974067 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988292 | ATGGTGAAAACCCAT[C/G]TCTACTAAAAATACA | 79058 |
| rs551998817 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981147 | TGTTTTGAAGAAACC[A/G]CAAGAGAGAAGGGCC | 79058 |
| rs552168285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989944 | TGGCGCACGCCATCA[C/T]GCCTGGCTAATTTTT | 79058 |
| rs552197975 | snp | C/T | 0.000199794 | 0.00999284 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010837 | CCCCGACCGCTACGT[C/T]CTACAGGGCTTCTTC | 79058 |
| rs552212399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979031 | AGCCTGCATTTGTTG[C/T]GGGGACCGTCCATAG | 79058 |
| rs552224431 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007762 | CAGGGTCTCTCCCCC[A/G]GGAACCCAGGCGTGC | 79058 |
| rs552333701 | snp | C/T | 4.9884e-05 | 0.00499395 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985495 | AAGTTTCTCATGTCT[C/T]ATACCCTCCAGGTTC | 79058 |
| rs552444461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999575 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 79058 |
| rs552452780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006130 | TTGCGGGTACACATG[C/T]GTGCTTGGGGTGTGT | 79058 |
| rs552590522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993908 | CTCCCCTTTGCCTAG[A/G]CTCTGGCCATCTGCC | 79058 |
| rs552644744 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987456 | GCCGGGCGGTGCCCC[C/T]GGGCGTGAACAGAAT | 79058 |
| rs552665655 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996537 | ATCTGGGGAGCTCAG[C/T]CGCGGCGACTTGAGC | 79058 |
| rs552675107 | in-del | -/C | 0.0277895 | 0.114554 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984995 | CACCTGCGTGCACAC[-/C]CCCCCCACACACCTG | 79058 |
| rs552706161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987806 | GAGCCGAGATCGCAC[C/T]ATTGCACTCTAGCCT | 79058 |
| rs552718356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983125 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 79058 |
| rs552756636 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983445 | ACAGGACGTGGATGG[C/T]GGGGCGTGGATGGCG | 79058 |
| rs552815681 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976210 | GCTGATGTCCTGCAC[C/G]TCCTGCTGACTTGTC | 79058 |
| rs552880216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978098 | CGCGTTCCCATTCCG[G/T]GGCGTCCCCCGGAGC | 79058 |
| rs552899904 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010446 | AGGCAGGAGAAAGGC[A/G]TGAACCCGGGAGGTG | 79058 |
| rs552953973 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012629 | GAGGAAGGGCCCGGC[A/G]GGCCTCGGAGCAGGG | 79058 |
| rs552986845 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977404 | CCCCGGCCCAGCCTG[A/G]CCCCGGCGAGCCCAT | 79058 |
| rs553017278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008884 | CCAGCCCTGCCCCCA[A/G]GACCTGGCCTTGGCC | 79058 |
| rs553024807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992531 | TGGCCACCCCTCAGC[C/T]CAGGCCTCCCCAGCC | 79058 |
| rs553034143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81997020 | TTCTGACTTCGCCCA[A/G]GAAGGAATTTAGGGG | 79058 |
| rs553136639 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017026 | GCTGCTGAGGAGGGG[C/G]CGCTGGTCCCCCCTG | 79058 |
| rs553154408 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012008 | GCAAGGGGAGCCGGG[-/C]TGCACGGGTGGTGTC | 79058 |
| rs553257371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013448 | GCTCGGCTCTAGCCT[C/T]GGGGCCTCTCGGGGT | 79058 |
| rs553263471 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017671 | CAGGAGCCAAGCCCT[A/G]GGCCAGGAGCTGGGG | 79058 |
| rs553286270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991696 | AGGCTCTGTCTAGCC[A/G]CTTGGCGGCTGGGCT | 79058 |
| rs553331404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015879 | GGCTTTGATCCCAGG[C/T]GGCACAATTGGGTTT | 79058 |
| rs553373153 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986553 | TCTTTTCATCGTTGG[C/T]TGGAAGTCTCTGTCC | 79058 |
| rs553392961 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006269 | TTGGGGGGCGTGTGC[A/G]TGTCCTTGCGGGTGC | 79058 |
| rs553410002 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981992 | TCTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC | 79058 |
| rs553456138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000621 | TTAATGTTTTGCCTG[C/T]GTGTGGTTTTTGGAC | 79058 |
| rs553517325 | snp | C/T | 1.86883e-05 | 0.00305676 | intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82012163 | ATCTGCAGGCCTGTC[C/T]TCCTTCGGGCGCATG | 79058 |
| rs553517507 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001106 | AGCCGGTGTGGGACT[C/G]GTGGGGCGGGGAGGA | 79058 |
| rs553551741 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976424 | ATGGCTAGCCTGGGG[A/C]TTTCCCCAGGTTTCT | 79058 |
| rs553589762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007564 | TGGCCGCCTGAGCAC[A/G]GCATGTCCTGGGGCC | 79058 |
| rs553648169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001873 | CCGGGGGTGTTGGTG[C/T]GCTTTATCCACAGTG | 79058 |
| rs553650137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008273 | CCAGGAGGGTTGTTC[A/G]CAGGGACTGCCAAGC | 79058 |
| rs553669428 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997683 | TTTAGTAGAGACAGG[A/G]TTTTACCATGTTGTC | 79058 |
| rs553677995 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010445 | GAGGCAGGAGAAAGG[C/T]GTGAACCCGGGAGGT | 79058 |
| rs553711533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002758 | AGATGGGGTTTTACC[A/G]TGTTTGTCAGGCTGA | 79058 |
| rs553715791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995516 | ATTGACTGTGCCCTC[A/G]CTAGAGGCAGCTTCT | 79058 |
| rs553775270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991266 | GCCCCCAGTGTGCCC[A/G]GCCCCTGGCTGGATC | 79058 |
| rs553841226 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989706 | ACGTTGCAGCTCCAC[C/T]GCGAGGGTGTCACTG | 79058 |
| rs553844173 | snp | C/G | 1.66399e-05 | 0.00288438 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011544 | TTTCTCCTCTGCAGT[C/G]GGGGACTTGCGAGAC | 79058 |
| rs553900363 | snp | A/G | 0.000976086 | 0.0220701 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995047 | CGGCCCTCGGAGCCC[A/G]GGCTGCCCCGAAACC | 79058 |
| rs553901862 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990134 | ACAGGTGTCATTAAT[A/T]TTAGTAATACGTGTA | 79058 |
| rs553918471 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985057 | TCCCCCCCACACACA[A/C]CCACGCACACACCTG | 79058 |
| rs553966320 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994400 | CTCCTCTTAGTGGGC[A/G]GCTTAAGATGAAAGC | 79058 |
| rs554093405 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010353 | GCTGACACGGTGAAA[C/T]CCCATCTCTACTAAA | 79058 |
| rs554104752 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999123 | GGCATTTATGGGTTT[A/T]GTGCCAAAAGAGGCA | 79058 |
| rs554165238 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994161 | GGCATGTGTGGGAGG[C/T]GTGCTGCATATACCT | 79058 |
| rs554166198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994015 | TTTTTCTCAGTGGGG[A/T]GGATTTCACGGTGGG | 79058 |
| rs554183485 | snp | C/G/T | 0.000329508 | 0.0128316 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015354 | CACGTGGGGACAGGC[C/G/T]GGGTAGGCTGCCTGG | 79058 |
| rs554256960 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017819 | CCCAGCAAGTCTGAT[A/G]ACTTCTACAGGCTCC | 79058 |
| rs554277647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983896 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGCT | 79058 |
| rs554299275 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992093 | GCCAGTACCCTGCTG[C/T]GAGCAGGCACCCGCG | 79058 |
| rs554365515 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978215 | GGCACCTTGTGACCG[C/T]GAATCAATTAAATGT | 79058 |
| rs554407216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014873 | AGCTAGGGAGGGGCC[A/G]GCTCCAGGCCCTCAG | 79058 |
| rs554432061 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986636 | AGCCAGGGGGTTCTC[A/G]CCCTCCCCGGGCCTC | 79058 |
| rs554470763 | snp | C/G/T | 0.0115278 | 0.0751731 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010361 | GGTGAAACCCCATCT[C/G/T]TACTAAAAATACAAA | 79058 |
| rs554498970 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000309 | CGCCCGTCGGGAGGC[A/G]CTGTTGGGGTGGGGT | 79058 |
| rs554519288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008408 | GGGCCGAGTGTGGGT[C/T]GGCGCAGTGCTGAGG | 79058 |
| rs554550680 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985143 | GCACACACACGCACA[C/T]CTGCACGCACATGCG | 79058 |
| rs554557291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988554 | AAAGCCCGGAGCCCC[C/G]AGCCTGCGGCCCTGG | 79058 |
| rs554570057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998583 | TACTATTCCTAACTT[C/T]CTGACATTTAAAAAA | 79058 |
| rs554664815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014191 | TGAGTGCCTGCTGGG[C/T]GCCCGCCCCTAGCCA | 79058 |
| rs554684430 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003647 | CTGAGGGTGTTCCCC[A/G]TGCTTTGGATGTAAA | 79058 |
| rs554702930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984318 | TGCCGCAAGGGCAGC[C/T]TGTAATCCCAGCACT | 79058 |
| rs554705458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003960 | TCACCGGAGCCCTGG[C/T]GGGGCAGGCCGGGCC | 79058 |
| rs554771735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003522 | ACTCGCTGGCAGGCC[C/T]GGGCCATGAGCATCG | 79058 |
| rs554780624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009772 | GGGGCGACTGAGGTA[C/T]AGCTCTGAGGGGGCC | 79058 |
| rs554832791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997164 | GGCTCCATGACAAGG[C/T]GGCAACTGTGTCAGC | 79058 |
| rs554839608 | in-del | -/C | 0.496416 | 0.0421803 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010547 | AAAAAAAAAAAAAAA[-/C]AAAAACCAGCACATT | 79058 |
| rs554869574 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000617 | CCCATTAATGTTTTG[C/T]CTGTGTGTGGTTTTT | 79058 |
| rs554897366 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988263 | GTCAGGAGTTCGAGA[C/G]CAGCCTGGCCAACAT | 79058 |
| rs554925609 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012552 | CCGCTTGGAGGTCTC[A/G]GCCCCCCTGGGCTGC | 79058 |
| rs554971960 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977184 | GGGGACTGCCCCAAA[A/C]CATAAGGTCAGGAGG | 79058 |
| rs555033895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991805 | GGCAGGGCGCATGCT[A/G]CTGCCTGGGCTCTCG | 79058 |
| rs555094029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992105 | CTGCGAGCAGGCACC[C/T]GCGGAAGCGCCCCAA | 79058 |
| rs555096683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996237 | GGGGCTGGGCTGCCC[C/T]GACCTCATCTCTGTG | 79058 |
| rs555116531 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987016 | GACAACAGTGACGGA[C/G]CCTAAGAGCAAAGCC | 79058 |
| rs555157319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987397 | CAAACAGCGCGGGGA[A/G]CAGAAGTCAGGAAAG | 79058 |
| rs555170959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997860 | AGATGGAGTTTTGCT[C/T]CTGTCGCCCAGGCTG | 79058 |
| rs555230655 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992697 | GTCCGGGTTCTGCTC[C/G]GGCGCATTTTGAGGC | 79058 |
| rs555234059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993187 | CTCATTTCAGGGAGG[C/T]AAGTCCTGCCCTTTT | 79058 |
| rs555255509 | snp | C/T | 3.32066e-05 | 0.00407458 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012238 | CTCCTCAGTCATCAC[C/T]CCTCCAAAAACAGTC | 79058 |
| rs555355121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014664 | TTGGCTTCGTTCCCC[A/G]GAGGGTGGTGCTGTT | 79058 |
| rs555372324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983103 | GCCTGCCTCGGCCTC[C/T]GAAAGTGCTGGGATT | 79058 |
| rs555411207 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976580 | GGTGCGGTGGCTCAC[A/G]TGTGTAATCCCAGCC | 79058 |
| rs555430595 | snp | G/T | 3.49443e-05 | 0.00417982 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996493 | GCGTCGGCTGGCCAG[G/T]CAGCCGCCAGCGCTC | 79058 |
| rs555554075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986383 | GCAGTGAGCCGAGAT[C/T]GCACTGCTGCACTCC | 79058 |
| rs555597090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015801 | GGCTCCCCAGCTTCC[A/G]GCGCCTCTCCAGGGC | 79058 |
| rs555631036 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975732 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCT | 79058 |
| rs555637237 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010748 | GGGAGGCCACGCCCT[A/G]GTCCCTGGTGCAGCT | 79058 |
| rs555644170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981823 | ACAGGCACGTGCCAC[A/G]CCTGGCTAATTTTTG | 79058 |
| rs555649471 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014764 | GGGGTTGACGTGGGC[C/T]TCCTTTCGGAAGCTC | 79058 |
| rs555717770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014785 | TCGGAAGCTCTTCCT[A/G]GCAACACTGAGTGGG | 79058 |
| rs555719636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010286 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGTG | 79058 |
| rs555743346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985916 | CTAAGGGGAGACGTT[C/T]GGTGCTGGGGGCAGG | 79058 |
| rs555782117 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015458 | TCTCCTGGTGTTCCC[A/G]AGTCCTGCCCGCCCC | 79058 |
| rs555890043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980092 | GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTCCC | 79058 |
| rs556025949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001220 | CCTGCCTGGGACCCC[C/T]GTGTGCCTGGCAGGG | 79058 |
| rs556049846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006246 | TCCTTGCGGGTGCAT[G/T]TGCATGCTTGGGGGG | 79058 |
| rs556054178 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002267 | TTTTATTTTATTTTA[-/T]TTTATTTTTTTGAGA | 79058 |
| rs556226279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006068 | ATGTCCTTGCGTGTG[C/T]GTGTCCTTGCGTGTG | 79058 |
| rs556250593 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993511 | AGCCACCGCGCCCGG[A/C]TGAGTCCTGCTCTTT | 79058 |
| rs556288441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999952 | CTGTTGAGTGGACAA[A/G]GGAGTGGGGAGTGAG | 79058 |
| rs556313839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993972 | CTGATGAGGGGCATC[C/T]GCAAGGAAGGCCTGA | 79058 |
| rs556313903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989216 | CTGTCTCAGAAATAA[A/G]TATTAAATAAATTTC | 79058 |
| rs556375721 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989568 | TGTGCTTCGAAGGGG[C/T]GTTCTGAGGCTGGGG | 79058 |
| rs556418187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994584 | GGAGCCCCCAGGCCA[C/T]GCACCACAGGCCAGG | 79058 |
| rs556456663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014573 | CCTTCCTCCCGGGCA[C/T]GGTGGTGCCGCCTCC | 79058 |
| rs556485679 | snp | C/T | 0.00117263 | 0.0241855 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994983 | GGCAGTGGCGGGAGA[C/T]TCGGGCTCTTGAAAG | 79058 |
| rs556568500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998297 | TTTTATAATATTGTG[A/G]ATAGTATCATGCTTC | 79058 |
| rs556718869 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006020 | GTCTGTGGTTTTCTT[C/T]TGTGTGCATGTCCAT | 79058 |
| rs556739666 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978144 | GCGGTGGCAGATGTC[A/C]CGGCCGTGGGGCCTG | 79058 |
| rs556748767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995930 | TGCCGGTGCCCGGAG[A/G]GCTTCCCTGGGCTCT | 79058 |
| rs556757625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983492 | ACGGGGATGGCGGGG[C/T]GTGGATGGCAGGGCG | 79058 |
| rs556793092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985041 | CCAACATGCACACAC[C/T]TCCCCCCCACACACA | 79058 |
| rs556888965 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976717 | GGAGTGCCAAGGCCC[A/G]GCTGAGCCATGGAGG | 79058 |
| rs556931297 | in-del | -/C | 0.000879894 | 0.0209565 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010028 | GTTCTCCTGCCTCAG[-/C]CCTCCCAAGTAGCTG | 79058 |
| rs556978303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004246 | AGCACTGTCTGCTGT[A/G]AGGCCGCGCGCCCGC | 79058 |
| rs556979074 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989047 | ACCCCGTCTCTACTA[A/C]AAATACAAAAAGCAG | 79058 |
| rs556993207 | snp | C/T | 3.33957e-05 | 0.00408616 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012194 | GATGGGCGAGGTCCA[C/T]GGTGCTTCCTAACAC | 79058 |
| rs556994070 | snp | C/T | 0.00614434 | 0.0550855 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009012 | GCCCGTGACACCCGC[C/T]GTCAGCCGCGCCCTC | 79058 |
| rs557016677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988518 | CCAGGGACAGCAGGA[A/G]GTGGTGGGGCCGTTG | 79058 |
| rs557030407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993131 | GTCGGGGCTGGGCCT[A/G]TCCTGGGTGTGGCAC | 79058 |
| rs557052055 | snp | C/T | 0.0012731 | 0.0251978 | downstream-variant-500B, splice-donor-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017407 | TTGTGCATCCCTCAA[C/T]GCCTTCCTGTCATGC | 79058 |
| rs557084421 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983867 | AGCATCTCATGTTTT[C/T]TTTTTTTTGAGCTGG | 79058 |
| rs557144606 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985134 | TGTAAACATGCACAC[A/G]CACGCACATCTGCAC | 79058 |
| rs557173245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013485 | CCCGGTGACGTGCCT[A/G]CCTGCCTGCCTGCCG | 79058 |
| rs557234594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009245 | AGGGTTTGCCCCATC[A/G]GGTGCTTGTGCTGCC | 79058 |
| rs557234731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014016 | TTGGGCTTCCTTCCA[C/T]TGGCTTTGGCAGGGC | 79058 |
| rs557357802 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016251 | TCAGCTGGCTTGGGG[-/C]TTGGGGTGGTCCCAT | 79058 |
| rs557359261 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982337 | GGGAACCAGTGAGTG[C/T]GATTTTGAGGCAGGT | 79058 |
| rs557381313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001153 | TGGGGGTAAACCAGC[A/G]GGGAGGAGGCTGGGC | 79058 |
| rs557395519 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982986 | GCCCAGCTTATTTTT[G/T]TGTATTTTTAGTAGA | 79058 |
| rs557395932 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975997 | AGCTTTACGGTTTAA[C/T]ACTGAATCTACTCAT | 79058 |
| rs557441249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995585 | GTGGCCAGCCAGGCC[C/T]GATCCCTGCCCACCC | 79058 |
| rs557481725 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976534 | AACAGCACCCATGCA[A/G]AGATGTCCTTAGACT | 79058 |
| rs557502726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996175 | TAGGTGTACCCAGGC[C/T]CTCATCATGGAGAGC | 79058 |
| rs557699653 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997088 | TGGCTGTGTCTGCTC[C/T]GGGATGAGGCCGTGT | 79058 |
| rs557702954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991729 | CATGTGGTGGGTGAT[G/T]CCCTCTGCGGGCCTC | 79058 |
| rs557746230 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987001 | CCAAAACGGAACTCA[A/G]ACAACAGTGACGGAG | 79058 |
| rs557905875 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991336 | CAGTGCTTGGGGGCT[A/G]GCTGAGTGCATCTCA | 79058 |
| rs558023525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981720 | GTCACCTAGGCTGGA[A/G]GGCAGTGGCATGATC | 79058 |
| rs558036355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985674 | TGCTGTGGTTACTGG[A/G]TCTGGTTCAGAGCTG | 79058 |
| rs558077386 | in-del | -/CT | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999078 | ACCTGACTTCCTCAG[-/CT]TCCTCACCTGCAGAA | 79058 |
| rs558187368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014567 | GTGCCGCCTTCCTCC[C/T]GGGCACGGTGGTGCC | 79058 |
| rs558187703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011038 | GAGGCATCCCAGTTC[A/G]CAGAGTGTCAGGCAG | 79058 |
| rs558204039 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991914 | TCCCCAGCACACAGC[C/T]GCGCCTTGCCGGAGC | 79058 |
| rs558210886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985336 | CCGGGGAGCCTCCAA[G/T]GCCCTCACTCCAGAG | 79058 |
| rs558217429 | snp | A/G | 2.32145e-05 | 0.00340686 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994960 | TGCTGTCCCGCAGCC[A/G]TCTCCAGGGCAGTGG | 79058 |
| rs558276326 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017705 | GAGCTAGTAGGTCAC[C/G]CCACATCCGTAGGGC | 79058 |
| rs558380421 | snp | A/G/T | 4.72604e-05 | 0.0048609 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015393 | TCCCTGCACAGAGGC[A/G/T]CAGACAGGGAGCCCA | 79058 |
| rs558426556 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003032 | GGTGCCCGTTTAGTA[C/G]AGATGGAGTTTTCAT | 79058 |
| rs558447970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006327 | TCCTTGCGGGTGCAC[A/G]TGTGCTTGGGTGCAT | 79058 |
| rs558449759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015779 | GTCCTCCCCGTGCCC[A/C]CTTCCTGGCTCCCCA | 79058 |
| rs558511205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003571 | GCCTGGGGGCGGCGC[C/T]GTCTCCTCTGGGTGG | 79058 |
| rs558516098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005865 | TGTGGGAAAACCGTC[C/T]GGGTACTTGGGGACA | 79058 |
| rs558556029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984344 | GCACTTTAGGAGGCC[G/T]AGGCGGGCAGATCAC | 79058 |
| rs558591448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978870 | AAGGCAGGTTGCAGA[A/G]CTACAGGGTTTGAAG | 79058 |
| rs558591556 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984997 | ACCTGCGTGCACACC[A/C]CCCCACACACCTGCA | 79058 |
| rs558634691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004725 | CCCTGCTGTGCCCCC[A/G]GCATCACCCCTGTCC | 79058 |
| rs558639276 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010251 | ACAGCACATTTGAGC[C/T]GGGCGTGGTGGCTCA | 79058 |
| rs558699007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998241 | CACCCAAAATGCTGG[A/G]ATTACAATTGTGAGC | 79058 |
| rs558704440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005277 | ACATGAGGCCGCGTG[A/T]AGTGGGCATCAGTTG | 79058 |
| rs558832547 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999215 | CTGTGTCCCCTGAGG[G/T]CCAGGCTGCCAGCTG | 79058 |
| rs558847384 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979767 | TGGAGAAATAGGATG[C/G]CTTGAAAACTGCAGG | 79058 |
| rs558872121 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994627 | GCCCCCGGCTGTCAG[G/T]TGCCTCCTTTTGGTG | 79058 |
| rs558896726 | snp | C/T | 7.10303e-05 | 0.00595904 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009190 | CAGCTCAAGAGTGAG[C/T]GGTGGGTGCCCCCTC | 79058 |
| rs558898219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999857 | GTCTGCACCGTGTTG[A/G]ATGTGGGGGCTCCCA | 79058 |
| rs558922370 | in-del | -/AAAA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987864 | AAAAAACAAAAAAAC[-/AAAA]GAAACAACAAGGCTG | 79058 |
| rs558966925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987053 | ACGGGCAGGGGTGAG[C/T]GGGACCCGAGGCAGG | 79058 |
| rs558966959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982197 | TGCTCTCAAACTCCT[C/G]ACCTCAAGTGATCTG | 79058 |
| rs559116972 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989317 | TTTCATAGTGGGTGG[C/T]GTTGCCAGCCCCACG | 79058 |
| rs559185007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002165 | GGCCTCTTTTCATCT[C/T]CTAAAGTATTTTTCT | 79058 |
| rs559198851 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989080 | GGGTGTGGTGGTGAG[A/G]GCCTGTAATCCCAGC | 79058 |
| rs559215757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012013 | GGGAGCCGGGCTGCA[C/T]GGGTGGTGTCCCCTG | 79058 |
| rs559242741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002996 | TTTCGTGTCTCAGCC[C/T]CCTGAATAGCTGGGA | 79058 |
| rs559270529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991827 | GGGCTCTCGTCAGCA[C/G]CTGTGTTTGCGCCCG | 79058 |
| rs559277183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007998 | ACGCTGCTGAGGTCA[A/G]TGCAGCTCCCGCCAG | 79058 |
| rs559399454 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016222 | TGGCTTGAGGACCCT[C/T]GAGGCCCCAGCCTTC | 79058 |
| rs559462459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016582 | AGCCTGTCCCTGGAC[C/G]TCAGAGCCAGCTGCC | 79058 |
| rs559486703 | snp | A/C | 1.66524e-05 | 0.00288547 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010776 | GCTCCGGCCGTCCCT[A/C]CAACCCTTCCACTTG | 79058 |
| rs559507910 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976607 | AGCCCTGTGGGAGGA[C/T]TGACTGATAACTGCA | 79058 |
| rs559561495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008472 | TTGAAATCACTGCCC[A/G]GGGCTCCGCGAGCTG | 79058 |
| rs559741070 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004331 | TTCTGGCCTTTCTCC[-/G]GCCCCCTTCCAGTTT | 79058 |
| rs559802195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991499 | TGTGGCCACACTCAG[A/G]GTGGGTCTGTGCATG | 79058 |
| rs559905929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007083 | GCAGCCCTACTGCAG[A/G]CGCCATATGTTCTCG | 79058 |
| rs559955203 | in-del | -/T | 0.00874735 | 0.0655527 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002880 | TCTTTTTAAAATAAC[-/T]TTTTTTTTTTTCGAG | 79058 |
| rs559998770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994618 | CTTGGGAGCGCCCCC[A/G]GCTGTCAGGTGCCTC | 79058 |
| rs560013744 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981348 | GGTTCAGTTGGTTGG[C/G]GGGGGCTTAGGGTTT | 79058 |
| rs560077755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999519 | GTAATCCCAGCTACT[C/T]GGGAGACTGAGGCAG | 79058 |
| rs560138243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994190 | CTGCCCACCCATGCA[C/T]GGGTCCAGCTGTGCC | 79058 |
| rs560158294 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984050 | GTAGAGGCAGGGTTT[C/T]ACCATGTTGGCCTGC | 79058 |
| rs560167491 | snp | A/G | 0.000178939 | 0.00945714 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995012 | AGCACGACGTGTTTC[A/G]TGGAAAAAGAGGGAG | 79058 |
| rs560177448 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006672 | AGGAGGCTGGGGAGG[A/G]GGGACGGGAATTCCC | 79058 |
| rs560196968 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984502 | GAATGGCGTGAACCC[G/T]GGAGGCGGAGCTTGC | 79058 |
| rs560254990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993607 | AAGCACACAGGTGGG[C/T]TCAGGCGGAGGCCGA | 79058 |
| rs560295277 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82018028 | CTTTTGTGCTTCCCA[C/T]CCTGGGGCCTGACTC | 79058 |
| rs560311930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009995 | GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAA | 79058 |
| rs560371296 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998145 | TTTATTTTTATTTTT[A/C]TTTTTCATAAAGACG | 79058 |
| rs560401480 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989097 | CCTGTAATCCCAGCT[A/G]CTTGGGAGGCTGAGG | 79058 |
| rs560424357 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013784 | GGACAGGGAATTGTG[A/G]GCAGTGTGGGGGCAC | 79058 |
| rs560433403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985454 | AGTCTGGGATTTAGA[A/T]GGAATAGTTGCTTTT | 79058 |
| rs560434476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010421 | GTAGTCCCAGCTGCT[C/T]GGGAGGCTGAGGCAG | 79058 |
| rs560435042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005457 | CAGGCTTCTGGAAGG[C/T]TCCTCCTGGCTCTCA | 79058 |
| rs560461191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985955 | TGCTTGATTCCCCTG[A/G]ATGGGATCATAAGGT | 79058 |
| rs560584716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010300 | TTTGGGAGGCCAAGG[C/T]GGGCGGATCATGAGG | 79058 |
| rs560616271 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987083 | GAGATGACGGAGCCT[A/G]AGAGCAAAGCGAAGC | 79058 |
| rs560669872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014351 | TCTGAAATGTTCCTC[A/G]TTGACAAATGGTCTT | 79058 |
| rs560693083 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976893 | TGGCTGGCGATGGGA[C/G]TGTTTCCTGAGGCTG | 79058 |
| rs560799840 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975600 | TTACAGGCACGCACC[A/G]CCATGCCCGGCTAAT | 79058 |
| rs560899090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997384 | GCTGGTGAACGCATC[A/G]GCCAGTCTTCAATCT | 79058 |
| rs560907646 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001326 | GGAGCCCCCACATCC[A/G]ACGCGGTGCAGACTC | 79058 |
| rs560918064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009026 | CCGTCAGCCGCGCCC[C/T]CTGCCTCCAGCCCGT | 79058 |
| rs560937006 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012964 | CTAATGGTTTCCTCT[A/T]CAAAGCCTCTTCAGA | 79058 |
| rs560947166 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977582 | TGGCCGCGTGGCTGC[A/G]CGTCCTGGCTGTTGC | 79058 |
| rs560981229 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009353 | GGCCCAGGGAGGGGC[A/G]TCCAGACCTTCCTGC | 79058 |
| rs561041914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004273 | CCGCAGGGCTGCCCC[C/T]GGCATCCCGGACAGC | 79058 |
| rs561178589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998106 | TGCTGGGATTACAGG[C/T]TTGAGCCACCGCGCC | 79058 |
| rs561377167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002978 | CTCCTGGGTTCAAGC[A/G]ATTTTCGTGTCTCAG | 79058 |
| rs561407605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983208 | CACTCCAGCTTCCGC[G/T]AGTGCAGCAGTGTTC | 79058 |
| rs561431264 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986644 | GGTTCTCGCCCTCCC[C/T]GGGCCTCAGTTTCCT | 79058 |
| rs561452039 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990478 | TCCGCCTGCCTGGTG[A/G]GCCTGTGTCTGAGTT | 79058 |
| rs561460429 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012444 | GGGCCGTGCGCCTCT[A/C/G]AAGTTGCTTCTGACA | 79058 |
| rs561536735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011389 | ACGGTGGCCCAGCCA[C/T]GCCGAGCACCTGGAG | 79058 |
| rs561556754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988082 | AGAATTGCTTGAACC[C/T]AGGAGGTGGAGGTTG | 79058 |
| rs561571129 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999511 | GGTGCCTGTAATCCC[-/A]AGCTACTCGGGAGAC | 79058 |
| rs561603229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007249 | CTCCCCTGCTACCAC[A/G]GCCCCGTGTGGGACC | 79058 |
| rs561661720 | snp | A/G | 0.000689744 | 0.0185579 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017444 | CAGAAAAGGGCCCCC[A/G]TCGTCTGCCCTGGCT | 79058 |
| rs561662085 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007782 | CCCAGGCGTGCTCGC[A/G]GCCCTCTGGAATGCA | 79058 |
| rs561681029 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987927 | CACTTTGGGAGGCTG[A/T]GGCGGGTGGATCACG | 79058 |
| rs561689701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995689 | TCCTGGCACCAGGGC[C/T]TCCTCCTTGCAGCCC | 79058 |
| rs561848283 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006861 | GGGCAGAGCTCACCA[A/G]TCAACAGGGCTGGGT | 79058 |
| rs561908681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016552 | AGTGGTTGGGGCCAG[C/T]GTCGGAGTCCAGCCA | 79058 |
| rs561924923 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013155 | ACTGAGCGGGATTCC[C/T]TGCAGCGGAGGCAGG | 79058 |
| rs561929424 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982420 | CCACTTGCTTACAAA[A/G]TGCAGCCGGTGCAGA | 79058 |
| rs561986475 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015546 | ATGAGAACCAGGTGC[C/T]TCTCTGCATCGGTGG | 79058 |
| rs562015703 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976114 | TTACTCCACAAGGAG[A/C]CACGGACCTTGACCA | 79058 |
| rs562086610 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979836 | ACGCTTCTGTGTGGG[A/G]ATATTGTTCCCAAGA | 79058 |
| rs562115828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010386 | TACAAAAAATTAGTC[A/G]GGAGAGGTGGCGCAC | 79058 |
| rs562181246 | snp | C/T | 0.040671 | 0.13668 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006108 | GCTTGGGGGCGTGTG[C/T]GTGTCCTTGCGGGTA | 79058 |
| rs562187721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000901 | GCCAGTCCCAGCAGA[C/T]GCCCCCCACAACTCG | 79058 |
| rs562248087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006390 | GCACATATGTGCATG[C/T]ATGTTTGCCCCAGAG | 79058 |
| rs562480958 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005029 | TCAGGGGAGGCCATC[C/T]GTGGCTGGGCGAGGG | 79058 |
| rs562542215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998890 | TGCATGCAGGCAGGC[A/G]GCCAGGTGCTGACCT | 79058 |
| rs562568585 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993283 | CAGTGGCGCGATCTC[A/G]GCTCACTGCAAGCTC | 79058 |
| rs562699875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989923 | CACCTGAGTAGCTGG[A/G]ATTACTGGCGCACGC | 79058 |
| rs562731448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013695 | GGGCTCCGGTAGCCC[A/G]GCAGCCCTCTGTGGC | 79058 |
| rs562760667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990301 | TCCTCGTGGACTGGG[C/T]GCTCTCCACTCTGCT | 79058 |
| rs562767021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988341 | TGGCTCATGCTTGTA[A/G]TCCCAGCTACTCAGG | 79058 |
| rs562798291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014269 | CCGTGTCGCCCACTG[C/G]CGGGGCCTCTCTGGG | 79058 |
| rs562860568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009871 | TGGCGCGCATGCCCT[C/T]AGTGGCCAGTTGATC | 79058 |
| rs562910360 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989669 | GGTGATTTCCTTGGA[C/T]GGACACTGCCACGTG | 79058 |
| rs562978817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984448 | CGTGGGTGGTGGCGG[A/G]TGCCTGTAGTCCCAG | 79058 |
| rs563020536 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976705 | CACATGGAGAGAGGA[C/G]TGCCAAGGCCCGGCT | 79058 |
| rs563072476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984006 | ACTACAGGTGCCCGC[C/T]ACCACACCCGGCTAA | 79058 |
| rs563083054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980580 | GGAAAGGAGGGCTTT[A/G]TTTCTCATAACCGGT | 79058 |
| rs563085184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978602 | AGGTGCACACGACTC[A/G]GAGTTTGCGGGAGCA | 79058 |
| rs563109446 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977481 | CTGGCGCGGGCTTTG[A/G]CGGCCCAAGGGCGGG | 79058 |
| rs563235997 | snp | C/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978174 | GGAAGCGATTTTTGC[C/G]GAGTCACTCACTGCA | 79058 |
| rs563244866 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997341 | GAAAAGGGGTGGTAA[A/C]TTCCGGGTTATGGCC | 79058 |
| rs563257643 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008496 | CGAGCTGCACGGCCC[A/G]GCTTTGTCAATTTCA | 79058 |
| rs563314240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003114 | TGGCCTCCGAAAGAG[C/T]TGGCATTACAGGCGT | 79058 |
| rs563334890 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983173 | GTGGTGGCTCCAGCC[A/G]TGACGGCCGGGGTCT | 79058 |
| rs563347941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980551 | GTCAACTGAAGAATG[C/T]GGTTCATATGTTTGG | 79058 |
| rs563388714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012744 | CCCGCTGGCCCCCCG[A/G]TCCCTGCTAGGAACG | 79058 |
| rs563418217 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985872 | AAGAGCAGGAATGTG[C/G]TTCTGTCCTTGTGGG | 79058 |
| rs563537131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003646 | GCTGAGGGTGTTCCC[C/T]GTGCTTTGGATGTAA | 79058 |
| rs563572160 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001480 | TGGAATGGCCACCAA[C/G]CGTGGCTGGCAGATG | 79058 |
| rs563725856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000772 | AGGTAGTTTTACTGG[C/T]GATCAGAACCGGGCG | 79058 |
| rs563761352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007679 | AGGGAGGCTCTGGAC[A/C]AGGCTGCAGAGGATG | 79058 |
| rs563772688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995844 | GTGGAGGGTGTGGAC[C/T]GGCAGGGGCCAGATG | 79058 |
| rs563840385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987135 | CCCGAGGCAGGAGGT[A/G]ACAGAGCCTAAGAGC | 79058 |
| rs563857852 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996351 | GGGAGAGGGTGAGCC[G/T]GGGCCGGGAGAGGGT | 79058 |
| rs563930351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015648 | AGCAGCCTCTGGGCA[A/G]TGTACCCTGGGCTTC | 79058 |
| rs563958076 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001702 | GCCCCTTCTGGCCTG[A/G]ACTCTCCTCCCCGTT | 79058 |
| rs563994106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016023 | CCAGCCCCACTCCCA[C/T]CCCCAGCCTGTGGCC | 79058 |
| rs563994179 | snp | C/G | 1.66676e-05 | 0.00288679 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010844 | CGCTACGTCCTACAG[C/G]GCTTCTTCCGCCCCA | 79058 |
| rs564000787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016642 | TGGGTCTGAGAGGGA[C/G]ATCTGCGGCCCCCAG | 79058 |
| rs564034441 | in-del | -/AGG | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004119 | ATTACTGTCAAGAAA[-/AGG]AGACCTCTGGGCAGT | 79058 |
| rs564070802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993064 | TGAAAAATAAAGGCC[A/C]CGAAACAAAAGAAAA | 79058 |
| rs564092305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984676 | TGTCTGTCCTGAGGC[C/T]GCAGTCAGGTTCGGT | 79058 |
| rs564180337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985111 | GCACATACCCGCACA[C/T]ACCTGCATGTAAACA | 79058 |
| rs564245179 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992529 | TCTGGCCACCCCTCA[C/G]CCCAGGCCTCCCCAG | 79058 |
| rs564245742 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006406 | ATGTTTGCCCCAGAG[C/T]GGAAGGAAAGTGAAT | 79058 |
| rs564305608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980378 | GCCTTACGAGGCTCT[C/T]CTGGGAGGAGTTTCT | 79058 |
| rs564313243 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981375 | GTTTCATTTTTATTT[A/C]TTTTTTATTTTATTA | 79058 |
| rs564346644 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986629 | TGCTGTGAGCCAGGG[A/G]GTTCTCGCCCTCCCC | 79058 |
| rs564349934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982032 | GGAGTGCAATGGCGC[A/G]ATCTTGGCACACTGC | 79058 |
| rs564462199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000203 | GGCGTGGGCCTCAGC[C/T]CCTTCCCTCCGTGAC | 79058 |
| rs564465424 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014449 | CCCAGGCACCGTGGT[A/G]CCTTCTCTCTCCCGG | 79058 |
| rs564541753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014630 | CTCCCGGGCGTCTTG[A/G]GCTGCAAGGGCTCCT | 79058 |
| rs564584146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006101 | CGTGTGTGCTTGGGG[A/G]CGTGTGTGTGTCCTT | 79058 |
| rs564594962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010137 | ATGTTGGCCCGGCTG[A/G]TCTCGAACTCCTGAC | 79058 |
| rs564638053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010311 | AAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCG | 79058 |
| rs564700350 | snp | A/G | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005633 | CCTCATTCCCCGCTG[A/G]CCCTCCGTCTGCTTG | 79058 |
| rs564784838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009811 | GGTCTGTGGATGGGA[C/T]GTGGGGGCGACTGAG | 79058 |
| rs564843038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978399 | GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT | 79058 |
| rs564892933 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009404 | CACTCCCACCCTGGA[G/T]GGTGCAGGTGAGGAG | 79058 |
| rs564916497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993363 | GGACCACAGGCGCCC[A/G]CCACCACGCCTGGCT | 79058 |
| rs564920024 | snp | A/G | 3.64173e-05 | 0.004267 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996845 | AGCAGGAGCGGGAGC[A/G]GGTAAAAGGGGCTCT | 79058 |
| rs564982908 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997289 | ACATCCACTCAACTA[C/T]ATGCACGTTAAGGGG | 79058 |
| rs564996503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998122 | TTGAGCCACCGCGCC[C/T]AGCCTAATTTATTTT | 79058 |
| rs565013468 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001130 | GGGAGGAGCCTGTCC[C/T]AGGGTTTTGGGGGTA | 79058 |
| rs565135789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993690 | ACCTGGACACTGCAG[C/T]ACCCTGCCCTCTGAC | 79058 |
| rs565187173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994127 | CATGTGCCCGTCTCC[C/T]GGGCTGCCATGCACA | 79058 |
| rs565195938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989338 | CAGCCCCACGGTGAG[A/G]GTGGAGTGCCTGGTG | 79058 |
| rs565209491 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017849 | CCAGGGCTTTCAAAC[C/T]GACCTACTGAGGTGG | 79058 |
| rs565243270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987736 | AAGTGGCTTTGGAGC[C/T]GGCTTTGGTGGTGGC | 79058 |
| rs565290663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981568 | ATTTTTAGTAGGGAC[A/G]GGGTTTCACCATGTT | 79058 |
| rs565300307 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986656 | CCCCGGGCCTCAGTT[C/T]CCTCACCTGTGCCCC | 79058 |
| rs565447975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988259 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 79058 |
| rs565472978 | snp | C/T | 0.000269094 | 0.0115963 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009068 | CCGTGGACCGGGAGC[C/T]GGTGGTGTGCCACCC | 79058 |
| rs565473391 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001114 | TGGGACTCGTGGGGC[A/G]GGGAGGAGCCTGTCC | 79058 |
| rs565556537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977791 | GTAGGCGGGCGGGGG[A/G]CGCTGCGCCGAGGCC | 79058 |
| rs565558428 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983944 | CTCACTTCAAGCTCC[A/G]CCTCCCGGGTTCACA | 79058 |
| rs565603963 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981761 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCGATTA | 79058 |
| rs565604227 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013645 | TCCAGGGGCCGGCCC[C/G]CGGCTTCCGAGAGGG | 79058 |
| rs565738181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011441 | GAATTCCCACCCCTC[A/G]GGGAAAGGCCCAGGA | 79058 |
| rs565776131 | in-del | -/A | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978525 | GCGAGACTCCATATC[-/A]AAAAAAAAAAAAAAA | 79058 |
| rs565933280 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007984 | GCTGCCCTGCCATGA[C/T]GCTGCTGAGGTCAGT | 79058 |
| rs566049443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980977 | CGAGATCAGCCTGGG[A/G]AACATAGTGAGACCC | 79058 |
| rs566177590 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014216 | TAGCCAGTTCTGTCG[C/T]CCTTCCTTTCCACCC | 79058 |
| rs566188170 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017469 | CTGGCTCAGCTGGAC[C/T]GCAGTGTCCAGGCCT | 79058 |
| rs566291953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015772 | TGGCGCTGTCCTCCC[C/T]GTGCCCCCTTCCTGG | 79058 |
| rs566307992 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976257 | GCCCCAAACGTTTAA[C/T]CAAGGATCCAGACTG | 79058 |
| rs566308172 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990973 | AGGACCTAGTTGCCA[A/C]GTGGTGAAAGGCAGG | 79058 |
| rs566326847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993822 | GTCTTCCTGTCCCAC[C/T]TGAGCCCTTGCAAGG | 79058 |
| rs566346825 | snp | A/G/T | 2.10338e-05 | 0.00324291 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015374 | AGGCTGCCTGGCTCA[A/G/T]TGCTCCCTGCACAGA | 79058 |
| rs566397212 | in-del | -/T | 0.0905309 | 0.192535 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997829 | TACTGAGGCACCCAC[-/T]TTTTTTTTTTTTTTG | 79058 |
| rs566458784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989062 | AAAATACAAAAAGCA[A/G]CTGGGTGTGGTGGTG | 79058 |
| rs566485859 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983765 | GGGTGCTGGGGAAGG[A/T]GGGACATGAGTCTTA | 79058 |
| rs566589173 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984985 | ACACACCCACACACC[A/T]GCGTGCACACCCCCC | 79058 |
| rs566592318 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979928 | GATAGGATGTGCGTG[A/T]CTATCCCACACGCGA | 79058 |
| rs566601619 | snp | C/T | 6.80758e-05 | 0.00583381 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009156 | GCTGACGGTGGACGA[C/T]GTGAGAAGACGCTTG | 79058 |
| rs566623489 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010343 | GACCATCCTGGCTGA[C/G]ACGGTGAAACCCCAT | 79058 |
| rs566626683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985218 | CATACCTGCACACAA[C/T]TGCACACCCCCGCAC | 79058 |
| rs566661122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009670 | ACAGCTCTGAGCGGG[C/G]CCCCTGTGAGGTCTG | 79058 |
| rs566691961 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978886 | CTACAGGGTTTGAAG[A/G]AGAGCCCAGGGTGTG | 79058 |
| rs566796493 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984948 | ACACCCGCACACACC[C/T]GCACACACCCCACAC | 79058 |
| rs566827172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013824 | GAACAAAGCCCCCCG[C/T]CCCTGCCTGAAACCT | 79058 |
| rs567110652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998202 | TCTCGAATTCCTGGG[C/T]TCAAGCGATCTTCTT | 79058 |
| rs567167183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987802 | CAGTGAGCCGAGATC[A/G]CACCATTGCACTCTA | 79058 |
| rs567174391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993435 | AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT | 79058 |
| rs567267862 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008538 | GCCAATTAGGGGTGA[C/T]GCTGTCCCTCCCGCA | 79058 |
| rs567328637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003204 | TAATCACAGCACTTC[A/G]GGAGACCGAGCTGGG | 79058 |
| rs567391056 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993048 | CCCAGGATTGAGGAC[A/G]TGAAAAATAAAGGCC | 79058 |
| rs567436515 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992490 | GCTGGCGGTCAGTGC[C/G/T]GGGGAAGGACTGTGA | 79058 |
| rs567599340 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017643 | AGTCTTTTGGGGGAA[A/G]TCACCTGCAACCCAG | 79058 |
| rs567645890 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991177 | CAGATTCATGAGCTC[A/G]GCCATGGAGGGGATT | 79058 |
| rs567701559 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016426 | CTGCCTTCACAGCAG[C/G]GGGGTGCTCTGCCCA | 79058 |
| rs567706058 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991573 | CCTGCCCGTCCCTGT[C/T]CATCCCTGTCCGTCC | 79058 |
| rs567712553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982297 | CAGTGTTCACCTGCC[C/T]GTGGTCTGTGTGGTG | 79058 |
| rs567780371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986885 | GTCTGCACGTCGGGT[A/C]TCAGTGGTCATGGGG | 79058 |
| rs567788733 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010484 | CAGTGAGCCGAGATC[A/C]TGCCACTGCACTCCA | 79058 |
| rs567810303 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975787 | TTTTTTTTTTGAGAC[A/C]GAGTCTTGCTCCGTC | 79058 |
| rs567842210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010926 | CCATGGGGCCTCTCC[C/T]GGCTCCTTCCTTCCA | 79058 |
| rs567885910 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994178 | TGCTGCATATACCTG[C/T]CCACCCATGCACGGG | 79058 |
| rs567922100 | snp | G/T | 2.52726e-05 | 0.00355467 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012136 | TTCTGCCCCACTTGA[G/T]GCGTCACCCCCATCT | 79058 |
| rs567926195 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995768 | CCAGGCTGGGGGAGA[C/G]ACGGTCAGGCATGGG | 79058 |
| rs567929999 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976350 | ACCAGGTGATGTGTG[C/G]CTCAGTAAGGTTCTG | 79058 |
| rs567973958 | snp | C/T | 3.59835e-05 | 0.00424152 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015312 | CCGAGCAGTGGCGAT[C/T]CCTCCCGAGTCAAGG | 79058 |
| rs567995716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008248 | AGACTGCAGGGTAGA[C/T]GGGACGGGACCAGGA | 79058 |
| rs568008855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980931 | AGCACTTTGGGTGCC[C/T]GAGGCGGAGGATTGC | 79058 |
| rs568112684 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015688 | CCGCAGCCTGGGTGT[G/T]AATCTTGGAGGCCCG | 79058 |
| rs568132797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981483 | TCCCAGGTTCAAGTG[A/T]TTCTTCTGCCTCAGC | 79058 |
| rs568142522 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001927 | GTGCCCAGCTCCAGA[C/T]GGGCTCATGGTCAGC | 79058 |
| rs568180696 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004965 | AGCTGCTCCCATGGA[C/G]CTGCGACCTGCTGCC | 79058 |
| rs568218312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001073 | ACCCCTGCTCACACC[C/T]GGCCCTCTGTGGCTG | 79058 |
| rs568281556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995462 | CCTGAGGCTGTGGCC[C/T]TCAGGGACCCTTACA | 79058 |
| rs568310793 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010345 | CCATCCTGGCTGACA[C/T]GGTGAAACCCCATCT | 79058 |
| rs568416547 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005735 | AACCCGAACCTCACT[C/G]AGCACAGAGAATTGG | 79058 |
| rs568417933 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990578 | GGGATCTTCCACGCC[C/G]AGCTCTGGGGGACAC | 79058 |
| rs568424801 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976530 | GCACAACAGCACCCA[C/T]GCAGAGATGTCCTTA | 79058 |
| rs568454118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010332 | CAGGAGATCGAGACC[A/G]TCCTGGCTGACACGG | 79058 |
| rs568543695 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978649 | CCCCAGGCCTGGGCA[C/G]GTGGAGGGCGCAGCC | 79058 |
| rs568645048 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007233 | TTCCGTAGAGGCCGC[G/T]CTCCCCTGCTACCAC | 79058 |
| rs568756749 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985264 | TATGCACACACGCAC[A/G]CACACCTGCACATAC | 79058 |
| rs568849874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993136 | GGCTGGGCCTGTCCT[A/G]GGTGTGGCACCTTGG | 79058 |
| rs568911874 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993380 | CACCACGCCTGGCTA[A/T]TTTTTTGTATTTTTA | 79058 |
| rs568917341 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999199 | GGCTGTTTCCCAGCC[C/T]CTGTGTCCCCTGAGG | 79058 |
| rs568973771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012505 | GGCCCCGGGTGGGAA[A/G]GGACCTGCTAGGCGG | 79058 |
| rs568975669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988960 | CACCTGTAATCCCAG[A/C]ACTTTGGGAGGCTGA | 79058 |
| rs568977945 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981881 | ATGTGGACCAGGCTG[G/T]TCTCAAACTCCTGAC | 79058 |
| rs568993090 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984239 | GTCAGCAGCATTCAC[C/G]CACCAGCCTGACCAC | 79058 |
| rs569005515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984809 | CCCACACACCCACAT[A/T]CCCGCACACCCGTAC | 79058 |
| rs569035450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008678 | GGGGTTTTTGCCGAC[A/G]CTCTAATTTGGCGGC | 79058 |
| rs569075977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014089 | CTGCCTCTGGGGACC[A/G]TCTGCCAGGACACAG | 79058 |
| rs569082539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978757 | AAGGCCACGGCTTTG[C/G]CTTTTTATGGAGAAG | 79058 |
| rs569139281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014515 | TGCTGCCTCCCTCCC[A/G]GGCTCTGTGGTGCCA | 79058 |
| rs569159573 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014906 | TGTGTCAGGGCAGGG[C/T]GGGCACCCCCACTTC | 79058 |
| rs569218953 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017566 | CCGCGTGGGTCTCCT[C/T]TTCGTTTTTAACCTA | 79058 |
| rs569237625 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017237 | GCCGAGTGCTTCAGC[C/G]GGGCTGGTGGGCGGG | 79058 |
| rs569262066 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975677 | CAAGATGGTCTCAAT[A/C]TCTTGACCTTGTGAT | 79058 |
| rs569283933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983382 | ATATGATCGGGGACC[C/T]GCCTTGTGCCTCTGC | 79058 |
| rs569351524 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976305 | AATAGGAACAGACTC[C/T]TCAAAAACGCCACTA | 79058 |
| rs569447778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977944 | GGTCCCGGGGGTCCC[A/G]AGTGGGGGCGGGGCG | 79058 |
| rs569491348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003904 | CTGGCGTAGTGATTC[A/G]TTGAAGCTCAGAGCC | 79058 |
| rs569544164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007431 | TGTCCCCTATGGCCC[C/T]CATCCTGGAGGCACC | 79058 |
| rs569551920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997715 | AGGATGGTCTCAATC[C/T]CTTGACCTTGTGATC | 79058 |
| rs569553210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996944 | GGTGGCGTGGCCGTG[A/G]TGCGGGCAGAGGAAC | 79058 |
| rs569601445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001675 | GGCTGCTGCAGGGCG[C/G]AGACCCCACTGGCCC | 79058 |
| rs569617266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992407 | GGAGGAGCCGCACAT[C/T]AAAGCCGGGCTGGCG | 79058 |
| rs569662075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012028 | CGGGTGGTGTCCCCT[A/G]CAGGTGGGCCTGCCC | 79058 |
| rs569812032 | snp | C/G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983054 | TCACCATGTTGGTCA[C/G/T]GCTTGTCTCAAACTC | 79058 |
| rs569821774 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002308 | CTGTCACCCAGGCTG[A/G]AGTACAATGGCACGA | 79058 |
| rs569853951 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987355 | GCTGCTTCCTGAGAC[A/G]AGAGTGGCAGAGGGC | 79058 |
| rs569942351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005154 | GAGGCCTGGGGGTGC[C/T]GAGTGTTCCGGAAAT | 79058 |
| rs569964530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981745 | ATGATCTCAGCTCAC[C/G]GCAACCTCTGCCTCC | 79058 |
| rs570000731 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982246 | ATTGCTGGGATTACA[A/G]GCATGAGCCACCGCG | 79058 |
| rs570041761 | snp | C/T | 6.25606e-05 | 0.00559253 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994976 | TCTCCAGGGCAGTGG[C/T]GGGAGACTCGGGCTC | 79058 |
| rs570112771 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986356 | AGGATCACTTGAGCC[A/G]TGGAGGCAGTTGCAG | 79058 |
| rs570174168 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996301 | CATGGGGCAGGAGAG[A/G]GTGAACCGGGGGCGG | 79058 |
| rs570180121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014745 | ACAGAGTTGCTGCCC[C/T]GTGGGGGTTGACGTG | 79058 |
| rs570183390 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005529 | TGAGGCGTGGCAAGG[-/C]CCCCAGGGACACCTG | 79058 |
| rs570227214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991545 | AGAGCTCTGCGGCCC[A/G]TCCCTGTCCATCCCT | 79058 |
| rs570264240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015796 | TTCCTGGCTCCCCAG[C/T]TTCCGGCGCCTCTCC | 79058 |
| rs570280868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986809 | GCTGGGCCTGCTCCC[A/G]TCTGACAGTAGTGCC | 79058 |
| rs570310841 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999889 | CTAGCCCGGCGTCAG[A/G]GTCCAGCCCCTCTGT | 79058 |
| rs570328220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016346 | AGCTGGGCGATGGGC[C/T]CATGGGGGCCGGGCA | 79058 |
| rs570378685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985231 | AACTGCACACCCCCG[C/T]ACACACCCACACACA | 79058 |
| rs570465952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978659 | GGGCAGGTGGAGGGC[A/G]CAGCCAGGAGGCTGT | 79058 |
| rs570546494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010468 | CGGGAGGTGGAGCTT[A/G]CAGTGAGCCGAGATC | 79058 |
| rs570551240 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979041 | TGTTGCGGGGACCGT[C/T]CATAGTGTGGTCTTG | 79058 |
| rs570559493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979354 | AACAGTCATATATTC[C/T]CTCCCAACTCTGGAG | 79058 |
| rs570571119 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985207 | ACATCCACACACATA[C/T]CTGCACACAACTGCA | 79058 |
| rs570606531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006158 | TGTGTGCATGTCCTT[A/G]TGGGTGCACGTGTGT | 79058 |
| rs570611585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980724 | GGTGGCTGATACAGA[C/T]GTACTTAATACGCTG | 79058 |
| rs570627321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998269 | AGCCACCTCACCAGG[C/T]CTGAAAGTTACTTTT | 79058 |
| rs570660016 | in-del | -/TATTTT | 0.0103295 | 0.0711199 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002554 | CCTCTGTGCCCAGCC[-/TATTTT]TATTTTTATTTTTAT | 79058 |
| rs570689205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998974 | CAACCGTGGGGACCT[C/T]GTGTCTGTGGGGTCC | 79058 |
| rs570770683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999581 | GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC | 79058 |
| rs570770820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993911 | CCCTTTGCCTAGGCT[C/T]TGGCCATCTGCCCCC | 79058 |
| rs570804804 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007221 | GGTGTGGGAGGTTTC[C/T]GTAGAGGCCGCTCTC | 79058 |
| rs570816272 | snp | C/T | 0.404559 | 0.196498 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009733 | TCTGAGCGGGCCCCC[C/T]GTGAGGTCTGTGGAT | 79058 |
| rs570854672 | in-del | -/CCT | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981863 | AGTGACGGGGTTTCA[-/CCT]CCATGTGGACCAGGC | 79058 |
| rs570877001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004750 | CTGTCCTCTGAGACC[C/T]CTGACTCTGCCCAGC | 79058 |
| rs571147458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989542 | TCTGAGTCCAGGGAC[A/G]GTGTAGGCGCTGTGC | 79058 |
| rs571222326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984144 | TGCAGGCGTGAGCCT[C/T]TGCGCCCCGCCCACG | 79058 |
| rs571260337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003831 | GCGTCCACGTGCTCC[A/G]CCGCCTGCCTCCGAG | 79058 |
| rs571260358 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997064 | GAGAAAGTAGCTTTA[C/G]TGAGACGGTGGCTGT | 79058 |
| rs571399699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988801 | TGTCTCAGGGCATCC[C/T]GGGCAGGGTTGCAGC | 79058 |
| rs571452549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017169 | GGAGGGCGGGGGTCC[A/G]GGTGCTGTGGCAGGG | 79058 |
| rs571473205 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017674 | GAGCCAAGCCCTGGG[C/T]CAGGAGCTGGGGGAG | 79058 |
| rs571593492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013915 | GTGTGCGGTCCGCGT[C/T]CTCAGGTCATGAGGA | 79058 |
| rs571657886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986972 | GGTTAAGCACGAGCA[C/T]GGAATTCTCCCTCCC | 79058 |
| rs571684650 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007225 | TGGGAGGTTTCCGTA[A/G]AGGCCGCTCTCCCCT | 79058 |
| rs571718928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006286 | GTCCTTGCGGGTGCA[C/T]GTGCGTGTTTGGGGG | 79058 |
| rs571756923 | snp | A/C | 0 | 0 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008288 | GCAGGGACTGCCAAG[A/C]CATCCCCAGGTGTCG | 79058 |
| rs571822892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983257 | CTGTGTTTTCCGAGC[A/G]TCTGCACTGGGGCTG | 79058 |
| rs572004302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003388 | GAGAGATCAAGACTG[C/T]AGTGAGCTGAGATTG | 79058 |
| rs572146210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990884 | ATACTGTGACTCGGG[G/T]GATACTGTAGCACGT | 79058 |
| rs572196807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003309 | AAAAATTAGTAGGGC[A/G]TGATGGTGTGTGCCT | 79058 |
| rs572210086 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985072 | CCCACGCACACACCT[C/G]TACACACACACCTAC | 79058 |
| rs572296461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985320 | TGCTGGTGCAGCCCT[G/T]CCGGGGAGCCTCCAA | 79058 |
| rs572335082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980308 | TTTTACAGTACTGTT[G/T]TCCTAACACTGGGGG | 79058 |
| rs572347918 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994026 | GGGGAGGATTTCACG[G/T]TGGGGAGTTGGAAAC | 79058 |
| rs572372952 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986585 | CAGTAAAAGGCTCAG[C/G]AGAATGGAAGGGACT | 79058 |
| rs572409311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989709 | TTGCAGCTCCACTGC[A/G]AGGGTGTCACTGTAG | 79058 |
| rs572524483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990155 | AATACGTGTAGTTAA[C/T]TCAGTATACCCAAAA | 79058 |
| rs572544592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014608 | CAGGCGCTGTGGTGC[C/T]GCCTCCCTCCCGGGC | 79058 |
| rs572572879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014952 | GGAGCCAGGCAGGGG[C/T]AGCCTGAGACATCCT | 79058 |
| rs572589796 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979653 | GGTGAGGACATTGAC[C/T]CATCTTTTTTGGGGG | 79058 |
| rs572818498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013589 | CCAGCTTTCACGTCT[C/G]TGGCAGAGCCCCACT | 79058 |
| rs572824806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978327 | AGAGATCAAGACCAT[C/T]CTGGCTAAAACGGTG | 79058 |
| rs572868104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978837 | AGAGCCAGGGGGTAG[C/G]TTGTGCTAGGCAAGT | 79058 |
| rs572896905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009786 | ACAGCTCTGAGGGGG[A/C]CCCCTGTGAGGTCTG | 79058 |
| rs572905469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984339 | TCCCAGCACTTTAGG[A/G]GGCCGAGGCGGGCAG | 79058 |
| rs572914264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002993 | GATTTTCGTGTCTCA[G/T]CCTCCTGAATAGCTG | 79058 |
| rs572975788 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003564 | GTGCTCAGCCTGGGG[A/G]CGGCGCCGTCTCCTC | 79058 |
| rs573067127 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998620 | AGTGGGTGTTGAACC[A/G]TTTCAGTGTTTTCAG | 79058 |
| rs573110354 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977359 | ACCCCGGGGCTCAGT[A/G]CCGCTCACCGGGGGT | 79058 |
| rs573127607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993637 | AGAGTTCCTGTCCCA[A/G]CATCCCGCTCTGTGC | 79058 |
| rs573153822 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009398 | GCAGCCCACTCCCAC[C/T]CTGGAGGGTGCAGGT | 79058 |
| rs573211910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999143 | CAAAAGAGGCAGACT[A/G]GGGGACTGTCATGCG | 79058 |
| rs573232000 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005640 | CCCCGCTGGCCCTCC[A/G]TCTGCTTGGGAGCTT | 79058 |
| rs573319914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997218 | GGCACAGAGCAGGGC[C/T]GCCCTGGGGTGGTGC | 79058 |
| rs573351390 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997888 | CTGGAGTGTGGTGGC[A/G]CACTTTCGGCTCACT | 79058 |
| rs573406777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987025 | GACGGAGCCTAAGAG[C/T]AAAGCCAAAGCCACG | 79058 |
| rs573421076 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992122 | CGGAAGCGCCCCAAA[G/T]CACTTCTTGCATTTC | 79058 |
| rs573483822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987431 | AACGTCTGGAAGGAA[A/G]TGCCCCTGGGCCGGG | 79058 |
| rs573536347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988138 | TGGGCAACAGAGCGA[A/G]ACTCTGTCTCAAAAA | 79058 |
| rs573549648 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997741 | TGATCCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 79058 |
| rs573578597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996308 | CAGGAGAGGGTGAAC[C/T]GGGGGCGGGAGAGGG | 79058 |
| rs573595373 | in-del | -/GT | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991430 | TCTGGGTGTGCTGGG[-/GT]GTAGGGATGGGCTGC | 79058 |
| rs573809119 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983107 | GCCTCGGCCTCCGAA[A/G]GTGCTGGGATTACAG | 79058 |
| rs573970675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015468 | TTCCCGAGTCCTGCC[C/T]GCCCCTTTCTGTGCG | 79058 |
| rs574066438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015821 | CTCTCCAGGGCCACT[C/T]GGGCAGCCCCTGCCC | 79058 |
| rs574077059 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985935 | GCTGGGGGCAGGGCT[A/C]CCCATGCTTGATTCC | 79058 |
| rs574095452 | snp | C/T | | | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015182 | AGGAGATGGAGGCGA[C/T]GTGGACTCTGGGAGG | 79058 |
| rs574099446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981909 | GACCTCAAGTGATCC[A/G]CCCGTCTTGGCCTCC | 79058 |
| rs574106252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010356 | GACACGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 79058 |
| rs574140705 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992107 | GCGAGCAGGCACCCG[C/T]GGAAGCGCCCCAAAG | 79058 |
| rs574160631 | in-del | -/CTGGGGTG | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013362 | AGGCCCCTGAGAGCA[-/CTGGGGTG]CTGCTGCCCTGTTTC | 79058 |
| rs574219038 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001235 | CGTGTGCCTGGCAGG[C/G]CAGGTGCTGTTGACC | 79058 |
| rs574235981 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011168 | ACCCAGAGGAAGGCA[C/T]CCTACCCCGGGAGGA | 79058 |
| rs574291065 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007032 | GGGTCCCCTGGCATC[A/T]CCCTCTGTCATTTGG | 79058 |
| rs574335126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980209 | GACGGTCTAGAACTC[C/G]TGACCTTGTGATCCG | 79058 |
| rs574348227 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010374 | CTCTACTAAAAATAC[A/C]AAAAATTAGTCAGGA | 79058 |
| rs574362249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007509 | GGACGTGGCAGCAGC[C/T]CACATTTCCCCCAGT | 79058 |
| rs574414283 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987845 | AGAGCAAAACTCCAT[C/T]TCAAAAAAACAAAAA | 79058 |
| rs574482039 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000019 | CACCCCATCCTCCCT[A/C]TGGGAACTCTGCCAA | 79058 |
| rs574547762 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993518 | GCGCCCGGCTGAGTC[C/G]TGCTCTTTCAAGTAG | 79058 |
| rs574558796 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005724 | CTGAAACCTTCAACC[C/T]GAACCTCACTCAGCA | 79058 |
| rs574571341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000482 | ACGCAGAGGGCCCGG[A/G]GCCACATGCCGCTGC | 79058 |
| rs574611255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989240 | AAATTTCTAAAAGCT[C/G]AGACCCAAGCTTTGT | 79058 |
| rs574632776 | snp | C/T | 0.000464576 | 0.0152339 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995004 | CTCTTGAAAGCACGA[C/T]GTGTTTCATGGAAAA | 79058 |
| rs574672606 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989649 | TGTGTATTTGGGGAC[A/C/T]CCTGGGTGATTTCCT | 79058 |
| rs574787640 | in-del | -/GGGGTCCCG | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977918 | ACCTGCGCTTCCGCT[-/GGGGTCCCG]GGGGTCCCGGGGGTC | 79058 |
| rs574843539 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010295 | AGCACTTTGGGAGGC[C/T]AAGGTGGGCGGATCA | 79058 |
| rs574895352 | in-del | -/CA | 0.0023933 | 0.0345097 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013885 | CTGCCCTGGTGTCCT[-/CA]CACAGTCACTTCTGT | 79058 |
| rs575017371 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977513 | CCGGGGCGCCGTGGG[C/T]GGGGAAAGGGCGGGG | 79058 |
| rs575018779 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014574 | CTTCCTCCCGGGCAC[G/T]GTGGTGCCGCCTCCC | 79058 |
| rs575054176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978161 | GGCCGTGGGGCCTGG[A/G]AGCGATTTTTGCCGA | 79058 |
| rs575124467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014788 | GAAGCTCTTCCTGGC[A/G]ACACTGAGTGGGGCA | 79058 |
| rs575156894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988045 | TTCCTGTAGTCCCAG[C/T]TACTCAGGAGGCTGA | 79058 |
| rs575220291 | snp | A/G | 0.000873574 | 0.0208812 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017436 | GCTTCCTCCAGAAAA[A/G]GGCCCCCGTCGTCTG | 79058 |
| rs575236031 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017713 | AGGTCACCCCACATC[C/T]GTAGGGCAGGGCCTG | 79058 |
| rs575305414 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015529 | GGCCTGTGGGGGCTA[C/T]GATGAGAACCAGGTG | 79058 |
| rs575369626 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991658 | CTGGGTTGAGAAGGC[C/T]GGAGCCTGCCCCAGG | 79058 |
| rs575395995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012873 | CCTGCTGGGCCGCCC[C/T]CCAGAGCCAGAAGCA | 79058 |
| rs575411138 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009945 | AGACGGAGTCTCTCT[C/G]TGTCGCCCAGGCTGG | 79058 |
| rs575467276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004253 | TCTGCTGTGAGGCCG[C/T]GCGCCCGCAGGGCTG | 79058 |
| rs575472452 | snp | A/G | 9.996e-05 | 0.00706895 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010840 | CGACCGCTACGTCCT[A/G]CAGGGCTTCTTCCGC | 79058 |
| rs575477026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004831 | CCCAGGCAGTGAGGC[A/G]GAAACCAGGCTGGGC | 79058 |
| rs575528034 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998015 | TATTTTTAGTAGAGA[C/G/T]GGGGTTTCACCATGT | 79058 |
| rs575543979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988397 | GAGGCGGAGGTTGTA[A/G]TGAGCTGAGATTGCG | 79058 |
| rs575551688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007751 | GGCTCCTGGCCCAGG[A/G]TCTCTCCCCCGGGAA | 79058 |
| rs575575374 | snp | C/T | 0.433963 | 0.169285 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009744 | CCCCTGTGAGGTCTG[C/T]GGATGGGACGTGGGG | 79058 |
| rs575623641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995183 | CAAAACCGAGTGTGG[C/T]GTGGCGCAAGCAAAG | 79058 |
| rs575658664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008372 | CCGACAGCTCTCGGC[C/T]GTTCTGTGTGAGGGG | 79058 |
| rs575671516 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976058 | TTATTGGGAAAACTT[A/G]ATGCTTGTGGTCTCA | 79058 |
| rs575721840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002901 | TTTTTTCGAGACAGG[A/G]TCTGTCTATGTTGCC | 79058 |
| rs575741722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003439 | GGCAACAGAGCGAGA[C/T]GCTGTCTCAAAACAG | 79058 |
| rs575747075 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996213 | GGCCTCTGCCTGCCT[G/T]TGGGCGTGGGGGCTG | 79058 |
| rs575756229 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976542 | CCATGCAGAGATGTC[C/G]TTAGACTCAGCAATG | 79058 |
| rs575810927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991755 | GCCTCCCTGAGCCCA[G/T]TGGCTCCTGGCCTGC | 79058 |
| rs575830195 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012643 | CAGGCCTCGGAGCAG[A/G]GCTCAGGGAGCCCCA | 79058 |
| rs575908489 | snp | C/T | 0.000997606 | 0.0223116 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016522 | TGGGAGCCGAGGAGC[C/T]GGCAGGTGAGTGTCA | 79058 |
| rs575939381 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976805 | GCTAAGCACATTCGA[C/T]GGCTGCGAGTCAGGA | 79058 |
| rs575964833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992288 | CGCTGGAATTTCCCC[C/T]GGGCCCTGGCGTCCT | 79058 |
| rs575964845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997099 | GCTCCGGGATGAGGC[C/T]GTGTCCGCTCCGGGA | 79058 |
| rs575969866 | snp | A/G | 0.00026798 | 0.0115723 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016901 | CTGGGGGCACCTCCC[A/G]TGGCGGCACTCACCA | 79058 |
| rs575970189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011756 | CTCCTGCAGCCCATG[A/G]TGTCTGTGTGGAGAC | 79058 |
| rs576151878 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980456 | GACCACGTGAGAATC[C/T]CAGGACCTGTGCTCT | 79058 |
| rs576191449 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981066 | TGAAGACTGTGCCAC[A/G]AAAACCCTGACTGTG | 79058 |
| rs576335869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990243 | GCAGAGTCCTTGAGA[C/T]CTGCATGTATGGTGC | 79058 |
| rs576394716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985358 | ACTCCAGAGTGAATA[A/G]GAGGGTAGCCTTCTC | 79058 |
| rs576434599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014568 | TGCCGCCTTCCTCCC[A/G]GGCACGGTGGTGCCG | 79058 |
| rs576578194 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994289 | CCGGCCACAGGCAAG[C/T]GGGCGTGAGCGGAGT | 79058 |
| rs576584069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015014 | CCTGTGCCTCCCTCA[A/G]AGGCCCTTCCCGGGC | 79058 |
| rs576628173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006361 | GGTGTGTGTGTATAT[A/G]CATGTCTGTGTGTGC | 79058 |
| rs576648146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015436 | CTGGCTGCCAAGCCT[A/G]CTTCCCTCTCCTGGT | 79058 |
| rs576649589 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010378 | ACTAAAAATACAAAA[A/C]ATTAGTCAGGAGAGG | 79058 |
| rs576695915 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000773 | GGTAGTTTTACTGGC[G/T]ATCAGAACCGGGCGC | 79058 |
| rs576705145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006807 | GAATCCACCTGGCGC[A/G]GGAGCGGCGCTGATG | 79058 |
| rs576711168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010684 | GATTGGGGGTGGCTG[C/T]TTCTGCCTGCCTCAG | 79058 |
| rs576772481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011044 | TCCCAGTTCGCAGAG[C/T]GTCAGGCAGGCTGGG | 79058 |
| rs576773007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009815 | TGTGGATGGGACGTG[A/G]GGGCGACTGAGGCAC | 79058 |
| rs576814770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997295 | ACTCAACTACATGCA[C/T]GTTAAGGGGTGGGGC | 79058 |
| rs576840316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004991 | CTGCCCGGGGCCGGG[A/G]GTCTGGGCCTCTTTG | 79058 |
| rs576868914 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978897 | GAAGGAGAGCCCAGG[A/G]TGTGTGCCAGGAAGA | 79058 |
| rs576940823 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979403 | GCCACACTCTCTCCA[A/G]ATGCCCTAAGGGAGA | 79058 |
| rs576946962 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980592 | TTTATTTCTCATAAC[C/T]GGTTGCAGCTTGCAG | 79058 |
| rs576982645 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983502 | CGGGGCGTGGATGGC[A/G]GGGCGTGTCAGGCTC | 79058 |
| rs577026860 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989205 | AGAGCAAGACTCTGT[C/T]TCAGAAATAAATATT | 79058 |
| rs577157067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014239 | TTCCACCCAGGACAG[C/T]CCCGTCCTGCACTGC | 79058 |
| rs577161619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994130 | GTGCCCGTCTCCCGG[A/G]CTGCCATGCACATCA | 79058 |
| rs577225822 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994549 | TCCTGCCAGCGGCCC[C/T]GAGACTGGAGGTCTC | 79058 |
| rs577280798 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993275 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTCACT | 79058 |
| rs577319871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983154 | CCGGGCAGTCAGGTT[G/T]TCTGTGGTGGCTCCA | 79058 |
| rs577441086 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977408 | GGCCCAGCCTGGCCC[C/T]GGCGAGCCCATCCAA | 79058 |
| rs577491493 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984421 | GTCTCTACTAAAAAT[A/G]CAAAAATTAGCCGTG | 79058 |
| rs577549120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983951 | CAAGCTCCGCCTCCC[A/G]GGTTCACACCATTCT | 79058 |
| rs577565785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992210 | TGGGTCTTGCCCCTG[C/T]GGACATTGGGACTTG | 79058 |
| rs577629311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987473 | GGCGTGAACAGAATC[C/T]AGTGCTCCCACAGGC | 79058 |
| rs577706115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012421 | TTGAGAGCCGGTGGG[C/T]TCCGAGGGGGCCGTG | 79058 |
| rs577792235 | snp | C/T | 0.000189889 | 0.0097421 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017027 | CTGCTGAGGAGGGGG[C/T]GCTGGTCCCCCCTGA | 79058 |
| rs577836707 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008904 | TGGCCTTGGCCCTGC[G/T]CTGGCCGGGGCCAGG | 79058 |
| rs577863043 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007316 | GGCCCTTGGGATGAC[-/G]GGTAGGAATCTAGGG | 79058 |
| rs577917553 | in-del | -/CTTTCCA | 0.00358779 | 0.0422022 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014221 | GTTCTGTCGTCCTTC[-/CTTTCCA]CTTTCCACCCAGGAC | 79058 |
| rs577962454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011239 | CCCAGACGGCCGGGC[A/G]GCAGCAGCCCAAGGT | 79058 |
| rs578021575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011691 | GTCCCAGCTGGGGCT[C/T]GTGGCAGCTTCTCCA | 79058 |
| rs578023225 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011284 | CCAGGGAAAGGGAAG[C/T]GCTTAGGCTGGGGCG | 79058 |
| rs578070247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007581 | CATGTCCTGGGGCCC[C/T]GTCTGGTGGTCAGGC | 79058 |
| rs578089575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982312 | CGTGGTCTGTGTGGT[A/G]GTGTCTGGTGGGAAC | 79058 |
| rs578096247 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015006 | CCCCTCAGCCTGTGC[C/T]TCCCTCAAAGGCCCT | 79058 |
| rs578118057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986775 | TGACTGTGCGTTGGG[C/T]GCGCTTGGTGGCCCC | 79058 |
| rs578122462 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983206 | GACACTCCAGCTTCC[A/G]CGAGTGCAGCAGTGT | 79058 |
| rs578132790 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988806 | CAGGGCATCCCGGGC[A/G]GGGTTGCAGCAGAGT | 79058 |
| rs578197146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991837 | CAGCACCTGTGTTTG[C/T]GCCCGGCTTTGTCAT | 79058 |
| rs578237926 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996335 | AGGGTGAGCCGGGGG[C/T]GGGAGAGGGTGAGCC | 79058 |
| rs745347099 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002223 | TCTTATGAGTACCTC[A/G]TGCTTTATATTTTCA | 79058 |
| rs745358133 | snp | C/T | 0.00016186 | 0.00899466 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995963 | GGTCCCGGTGCAAGG[C/T]GCACCTGTCCTGGCT | 79058 |
| rs745374119 | snp | A/G | 1.78883e-05 | 0.00299062 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015219 | TTTTGGGGTCCATCC[A/G]GAGGCCGAGCCTCTC | 79058 |
| rs745414533 | snp | A/G | 1.79277e-05 | 0.00299392 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015143 | GTGCCTGGGACCAGA[A/G]CAGAGAACACGCTTG | 79058 |
| rs745472754 | snp | C/T | 0.000134402 | 0.00819651 | synonymous-codon, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017313 | CTGCACTACAGCCAG[C/T]AAGAGGTGAGAGCTG | 79058 |
| rs745625245 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008728 | CATGGAGACCCTGAC[A/G]TGGCCTGAGCCAGAC | 79058 |
| rs745656872 | snp | C/G | 3.34532e-05 | 0.00408968 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011641 | CCACTCCTGCCTCCA[C/G]TGCTCGGGGCCTTGG | 79058 |
| rs745664984 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007021 | CTCCACACACAGGGT[C/G]CCCTGGCATCTCCCT | 79058 |
| rs745709769 | snp | A/C/T | 3.32073e-05 | 0.00407465 | missense, synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011575 | TTCGTGAGGAGCCAC[A/C/T]TGGGGAACCCCGAGC | 79058 |
| rs745710823 | snp | A/G | 0.000183994 | 0.00958975 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985481 | TTTTCTTCCTAAGGA[A/G]GTTTCTCATGTCTTA | 79058 |
| rs745744274 | snp | C/T | 3.51296e-05 | 0.00419089 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996444 | GAAGTGCTACGACCC[C/T]GTGGGCAAGACCCCA | 79058 |
| rs745769115 | snp | A/C | 1.65479e-05 | 0.0028764 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016760 | GATGGTGAGTGGACC[A/C]CTCCTCAGAGGCTCA | 79058 |
| rs745853989 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983234 | TGTTCACGCCCCAGT[A/C]GTTCTCTCTGTGTTT | 79058 |
| rs745879216 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976088 | AGAGAATGACCTCAC[A/G]CATGCCTTAATTACT | 79058 |
| rs745898035 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013844 | GCCTGAAACCTGCGT[C/T]CTGGCCCTGGGCATC | 79058 |
| rs745909970 | snp | A/G | 3.74953e-05 | 0.00432969 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996376 | GAGGGTGAGCCGGGG[A/G]TAGGCACCACAAGGT | 79058 |
| rs745916425 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005312 | CTGGGGTTTGGTCTC[A/G]GAGGCCTGCGGGGCA | 79058 |
| rs745952406 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012464 | TGCTTCTGACACGGC[C/T]TTCCGGCCTCCTCTG | 79058 |
| rs745967501 | snp | C/T | 8.14963e-05 | 0.00638291 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009480 | TCCTTCCCCTCCTCA[C/T]CACAGGAAGCGCCTG | 79058 |
| rs746020195 | snp | C/G | 2.63877e-05 | 0.00363224 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009213 | GCCCCCTCAGTGCCT[C/G]CCGGCATCTTCGCGC | 79058 |
| rs746037363 | snp | C/G | 1.75326e-05 | 0.00296074 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015043 | GCCCTGCTCTGGCTG[C/G]GGGGACGGTGTGACC | 79058 |
| rs746038026 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006267 | GCTTGGGGGGCGTGT[A/G]CGTGTCCTTGCGGGT | 79058 |
| rs746138810 | in-del | -/AGCAGGAGCGGGAGCGGGATCCCC | 1.72481e-05 | 0.00293662 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996799 | CCCAGCAGGAGCAGG[-/AGCAGGAGCGGGAGCGGGATCCCC]AGCAGGAGCGGGAGC | 79058 |
| rs746194278 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012414 | AAAGCCTTTGAGAGC[C/T]GGTGGGTTCCGAGGG | 79058 |
| rs746202278 | snp | A/C | 3.34029e-05 | 0.00408661 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994851 | CCCCGGCGGGGCCAC[A/C]CCAGTCTGCGTGTAC | 79058 |
| rs746206862 | snp | G/T | 1.66211e-05 | 0.00288275 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012280 | CACGCAGACCCTCTT[G/T]CAGGTACCTGAGGGC | 79058 |
| rs746218180 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997055 | CAGGTGGTAGAGAAA[A/G]TAGCTTTACTGAGAC | 79058 |
| rs746230332 | snp | C/T | 6.35977e-05 | 0.00563869 | synonymous-codon, nc-transcript-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017107 | CCCAAGTGGCTGAAG[C/T]TGCCGGGTACTGCGG | 79058 |
| rs746239620 | in-del | -/TTTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009916 | ATTTAGAATGAAACC[-/TTTT]TTTTTTTTTGAGACG | 79058 |
| rs746259476 | snp | C/T | 1.66879e-05 | 0.00288855 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994786 | CTGGTTGAGCTGCCC[C/T]GGGGTACCTGATGGT | 79058 |
| rs746294503 | snp | A/G | 1.71481e-05 | 0.0029281 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010913 | GGGGGGCAGGGGCCC[A/G]TGGGGCCTCTCCCGG | 79058 |
| rs746299709 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981524 | GCTGGGATTACAGGC[A/G]TGCGCCATCATGCCC | 79058 |
| rs746317148 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999280 | TGAGCTCCTGCTGAC[A/G]TAGTGGGCCTGGAAG | 79058 |
| rs746326324 | snp | A/G | 1.69887e-05 | 0.00291446 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996615 | GGAGAAGCAGAGCAC[A/G]AGGGCACCCGCAGCT | 79058 |
| rs746350250 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986518 | TGAATGTGTAAAAAT[C/T]GGTGCTTTGTCAATT | 79058 |
| rs746536492 | snp | A/G | 1.74108e-05 | 0.00295044 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996805 | CAGGAGCAGGAGCAG[A/G]AGCGGGAGCGGGATC | 79058 |
| rs746564302 | snp | A/G | 2.26935e-05 | 0.00336842 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017126 | CGGGTACTGCGGCTG[A/G]GTGGAAGGTGGGGTG | 79058 |
| rs746572416 | snp | C/T | 4.98326e-05 | 0.00499138 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011562 | GGACTTGCGAGACTT[C/T]GTGAGGAGCCACCTG | 79058 |
| rs746600244 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990291 | CTGGGCCGGGTCCTC[C/G]TGGACTGGGCGCTCT | 79058 |
| rs746738639 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989551 | AGGGACAGTGTAGGC[A/G]CTGTGCTTCGAAGGG | 79058 |
| rs746745760 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985275 | GCACGCACACCTGCA[C/G]ATACCTGCACACTCA | 79058 |
| rs746796412 | snp | A/G | 9.68195e-05 | 0.00695704 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983649 | CCGCTTCCCGGAGCC[A/G]TGAGGGGCCTGAGAA | 79058 |
| rs746835737 | snp | A/C | 1.80624e-05 | 0.00300514 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983586 | TCGACCTTTCTCTCC[A/C]GTGGAGATTTGCCAA | 79058 |
| rs746857481 | snp | C/T | 2.23217e-05 | 0.00334071 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016446 | TGCTCTGCCCACACC[C/T]GGCCCCTGAGCCCCC | 79058 |
| rs746862778 | snp | A/G | 6.39502e-05 | 0.00565429 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996033 | CACGACGCTGCAGTC[A/G]CTGGGCCTGACCGGG | 79058 |
| rs746881953 | snp | G/T | 1.70554e-05 | 0.00292017 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009458 | CCATTCTGACCAGAA[G/T]CCCTGTTCCTTCCCC | 79058 |
| rs747029609 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997262 | GCTCAGGGCATGGCC[A/G]TGGTCACATTTACAT | 79058 |
| rs747052950 | snp | A/G | 2.36298e-05 | 0.0034372 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009191 | AGCTCAAGAGTGAGC[A/G]GTGGGTGCCCCCTCA | 79058 |
| rs747083050 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007097 | GACGCCATATGTTCT[C/T]GGGGTGACTCAGGTG | 79058 |
| rs747114459 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977591 | GGCTGCGCGTCCTGG[C/T]TGTTGCCGATAAAGT | 79058 |
| rs747131057 | snp | C/T | 1.66101e-05 | 0.0028818 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012267 | TCCTGGACGACCACA[C/T]GCAGACCCTCTTTCA | 79058 |
| rs747217798 | snp | A/G | 1.72222e-05 | 0.00293442 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017025 | AGCTGCTGAGGAGGG[A/G]GCGCTGGTCCCCCCT | 79058 |
| rs747241188 | in-del | -/A | 1.6633e-05 | 0.00288378 | intron-variant, frameshift-variant | ASPSCR1 | GRCh38.p7 | 17:82012208 | ACGGTGCTTCCTAAC[-/A]CGTAGGTGCCTTCTC | 79058 |
| rs747243769 | snp | A/G | 3.36276e-05 | 0.00410032 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016954 | AGGTACATGTCCAGG[A/G]CCGCCGGGTCCCCTT | 79058 |
| rs747248790 | in-del | -/TTT | 0.000170721 | 0.00923751 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010078 | CACTAGCTCGGCTAA[-/TTT]TTTTTGTTGTTTTTT | 79058 |
| rs747285149 | snp | A/G | 3.42918e-05 | 0.00414062 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985639 | TGGGGGCTCTTCCCT[A/G]CCCTGTTTGCTGGGG | 79058 |
| rs747342381 | snp | A/G | 1.70723e-05 | 0.00292162 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996595 | CCCTGCTGCGAGCAC[A/G]CTCAGGAGAAGCAGA | 79058 |
| rs747390436 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009916 | ATTTAGAATGAAACC[-/T]TTTTTTTTTTTTGAG | 79058 |
| rs747441094 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989037 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 79058 |
| rs747481008 | snp | C/T | 1.66454e-05 | 0.00288486 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010784 | CGTCCCTCCAACCCT[C/T]CCACTTGTCTGGCCT | 79058 |
| rs747567869 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981567 | TATTTTTAGTAGGGA[C/T]GGGGTTTCACCATGT | 79058 |
| rs747582679 | snp | A/G | 1.64806e-05 | 0.00287054 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979258 | AGTTTGCTCCAGCTC[A/G]GCAGCAGGGTCTGAG | 79058 |
| rs747601472 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981640 | CGCCTTGGTCTTCCA[A/G]AGTGTTGGGATTACA | 79058 |
| rs747660580 | snp | C/T | 1.67668e-05 | 0.00289537 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996689 | GCCCTCCTGGGCCCA[C/T]GAGGCCTCTGACATC | 79058 |
| rs747665753 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004482 | GGGCAGAAGCATGCA[A/G]GGGCTTCACCTGCAG | 79058 |
| rs747666860 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992106 | TGCGAGCAGGCACCC[A/G]CGGAAGCGCCCCAAA | 79058 |
| rs747711196 | snp | A/G | 0.000101102 | 0.0071092 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011492 | GTGCTGGGGCAGCCC[A/G]GGGCTGGCGTGGTGG | 79058 |
| rs747764370 | snp | C/T | 1.66988e-05 | 0.00288949 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010857 | AGGGCTTCTTCCGCC[C/T]CAGCGAGACAGGTGG | 79058 |
| rs747832563 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011177 | AAGGCACCCTACCCC[A/G]GGAGGAGGGCAGTGG | 79058 |
| rs747833748 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982421 | CACTTGCTTACAAAG[C/T]GCAGCCGGTGCAGAG | 79058 |
| rs747848543 | snp | C/T | 1.80328e-05 | 0.00300268 | stop-gained, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015318 | AGTGGCGATCCCTCC[C/T]GAGTCAAGGCTGGGC | 79058 |
| rs747857076 | snp | C/T | 1.87051e-05 | 0.00305813 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983576 | AGGAGCGTGCTCGAC[C/T]TTTCTCTCCAGTGGA | 79058 |
| rs747868020 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004018 | AGGGAAAAACACAAA[C/T]CCTCAGAGACGCTGG | 79058 |
| rs747895024 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994694 | GGCCTGGGCCTGGGA[C/T]GCTGTCCTGGGTGGG | 79058 |
| rs747908456 | snp | C/T | 1.64974e-05 | 0.00287201 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979290 | ATATCTGTGCCCCTG[C/T]CCCCTGAACATACTG | 79058 |
| rs747947379 | snp | A/G | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017604 | TTTACACTTCCTCCA[A/G]GGAGAACAGAAGTGC | 79058 |
| rs747959923 | snp | C/T | 9.6251e-05 | 0.00693659 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995983 | CTGTCCTGGCTGCTC[C/T]TCCTGCAGGTGACGG | 79058 |
| rs747972818 | snp | C/T | 0.000279619 | 0.0118208 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009097 | CCCGACCTGGAGGAG[C/T]GGCTGCAGGCCTGGC | 79058 |
| rs748152664 | snp | C/G | 1.68522e-05 | 0.00290272 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985622 | GGTGAGCATCAGTGG[C/G]CTGGGGGCTCTTCCC | 79058 |
| rs748237432 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995227 | GACCCTCCTAGCGCT[C/T]GTCCCTGGCCTCACA | 79058 |
| rs748263712 | in-del | -/GGT | 3.68895e-05 | 0.00429458 | cds-indel, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015111 | GCTCCATTCACCCTG[-/GGT]CCCTCGCTGAAACGG | 79058 |
| rs748275712 | snp | A/G | 1.67846e-05 | 0.0028969 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:82016940 | CTTCGCCTCCCCACA[A/G]GTACATGTCCAGGGC | 79058 |
| rs748292573 | snp | C/T | 1.65762e-05 | 0.00287886 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985530 | CGCTTTGCAGCTGGA[C/T]GATGGCTCGAGGTTG | 79058 |
| rs748306495 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008378 | GCTCTCGGCTGTTCT[C/G]TGTGAGGGGGGACGG | 79058 |
| rs748347591 | snp | C/T | 1.72656e-05 | 0.00293812 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996540 | TGGGGAGCTCAGCCG[C/T]GGCGACTTGAGCCGT | 79058 |
| rs748424534 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016143 | GCATCCGCCAGGACC[C/T]GCCACGCCTGGCCCC | 79058 |
| rs748454604 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989966 | CTAATTTTTGTATTT[G/T]TTTTAGTAGAGACAG | 79058 |
| rs748463491 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979148 | CCGCCAGCCCTGCAC[A/G]CTCAGCAGTTCACCA | 79058 |
| rs748511827 | snp | C/T | 3.33089e-05 | 0.00408085 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010772 | TGCAGCTCCGGCCGT[C/T]CCTCCAACCCTTCCA | 79058 |
| rs748515989 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002118 | CTCAGCCTCCCGAGT[A/G]GCTGGGACTGCAGGT | 79058 |
| rs748526490 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986052 | CAAGAAATTCTCCCA[A/T]CTCAGCCTCCCAAAG | 79058 |
| rs748608902 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007223 | TGTGGGAGGTTTCCG[C/T]AGAGGCCGCTCTCCC | 79058 |
| rs748611772 | snp | A/G | 1.79548e-05 | 0.00299617 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015136 | TGAAACGGTGCCTGG[A/G]ACCAGAGCAGAGAAC | 79058 |
| rs748748207 | snp | C/G | 2.36186e-05 | 0.00343639 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977685 | AGGCTCCGCGGTGTC[C/G]GTGCTGGCCCCGAAC | 79058 |
| rs748782188 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979271 | TCAGCAGCAGGGTCT[A/G]AGTATATCTGTGCCC | 79058 |
| rs748796428 | snp | G/T | 1.66344e-05 | 0.0028839 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010810 | GGCCTAGGTGGCTCT[G/T]AGGGTCCTGTTCCCC | 79058 |
| rs748811968 | snp | A/G | 1.98242e-05 | 0.00314828 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983567 | AGGTTTCAGAGGAGC[A/G]TGCTCGACCTTTCTC | 79058 |
| rs748837492 | snp | C/G | 2.63203e-05 | 0.0036276 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995967 | CCGGTGCAAGGCGCA[C/G]CTGTCCTGGCTGCTC | 79058 |
| rs748891853 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000935 | TCCCGGCAGCTGGCA[C/T]GAGGGCCGCTCCTGA | 79058 |
| rs748911313 | snp | C/G | 0.000393391 | 0.0140193 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015235 | GAGGCCGAGCCTCTC[C/G]AAGCACTGGTCAGCC | 79058 |
| rs748962513 | snp | A/G | 1.6517e-05 | 0.00287372 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017365 | GCCAGCCACAGGACC[A/G]CCTCCTCTGCCAGCA | 79058 |
| rs749077643 | snp | A/G | 0.000155231 | 0.00880861 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009075 | CCGGGAGCCGGTGGT[A/G]TGCCACCCCGACCTG | 79058 |
| rs749132095 | snp | A/G | 2.09457e-05 | 0.00323611 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009006 | GGCCCAGCCCGTGAC[A/G]CCCGCCGTCAGCCGC | 79058 |
| rs749149047 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995000 | CGGGCTCTTGAAAGC[A/G]CGACGTGTTTCATGG | 79058 |
| rs749195156 | snp | A/G | 3.34286e-05 | 0.00408818 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016856 | CCATCTGCGGCCGAT[A/G]TGCTGGTGGCCAGGT | 79058 |
| rs749301332 | snp | A/G | 1.72502e-05 | 0.0029368 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996521 | CTCCACTTCCCTTGG[A/G]ATCTGGGGAGCTCAG | 79058 |
| rs749324981 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986405 | CTGCACTCCAGCCTG[A/G]GCAACAGAACGAGAC | 79058 |
| rs749426350 | snp | A/G | 2.18668e-05 | 0.00330649 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016770 | GGACCCCTCCTCAGA[A/G]GCTCAGGGTGAGCTT | 79058 |
| rs749456130 | snp | A/G/T | 3.73296e-05 | 0.00432015 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996385 | CCGGGGGTAGGCACC[A/G/T]CAAGGTGCTTCCCTT | 79058 |
| rs749456696 | snp | A/G | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017686 | GGGCCAGGAGCTGGG[A/G]GAGGAGCTAGTAGGT | 79058 |
| rs749546618 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016611 | CCCGGGAGGGCGTTC[A/G]GTCTGGGGCCTCCTT | 79058 |
| rs749594577 | snp | A/C | 0.000567376 | 0.0168335 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977655 | GCGGAAAATGGCGGC[A/C]CCGGCAGGCGGCGGA | 79058 |
| rs749602936 | snp | C/T | 0.000381432 | 0.0138047 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009490 | CCTCACCACAGGAAG[C/T]GCCTGGAAGAAGCCC | 79058 |
| rs749633215 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008580 | GCAGAGGGAGGGGCC[A/G]GCTTGTTCCCTGGGG | 79058 |
| rs749691909 | snp | A/G | 0.000108079 | 0.00735036 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015050 | TCTGGCTGGGGGGAC[A/G]GTGTGACCCACTTTC | 79058 |
| rs749714196 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979592 | ACGATTTATCATTAC[A/G]TCTTCAAAGACCAGG | 79058 |
| rs749730438 | in-del | -/AGCAGG | 0.000393947 | 0.0140292 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996787 | CGGGCCAGGATCCCC[-/AGCAGG]AGCAGGAGCAGGAGC | 79058 |
| rs749744839 | snp | C/G | 2.14816e-05 | 0.00327724 | splice-donor-variant, missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017114 | GGCTGAAGCTGCCGG[C/G]TACTGCGGCTGGGTG | 79058 |
| rs749746317 | snp | C/G | 1.67464e-05 | 0.0028936 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994861 | GCCACCCCAGTCTGC[C/G]TGTACACGAGGGATG | 79058 |
| rs749759526 | snp | C/T | | | stop-gained, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996787 | TCGGGCCAGGATCCC[C/T]AGCAGGAGCAGGAGC | 79058 |
| rs749763768 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995334 | GCCAGGACATTCCCC[G/T]CATTTATCCCCATTT | 79058 |
| rs749810397 | snp | A/C | | | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017038 | GGGGCGCTGGTCCCC[A/C]CTGAGCCCATCCCAG | 79058 |
| rs749871516 | snp | A/G | 2.25482e-05 | 0.00335761 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009157 | CTGACGGTGGACGAC[A/G]TGAGAAGACGCTTGG | 79058 |
| rs749878638 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985828 | GTTCTGAGTTTCCTG[A/G]GCCCAGCGGCCCAGC | 79058 |
| rs749929584 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015934 | GTGTCCCTGGGCCCC[C/T]GGCTGGAGGCTGAGG | 79058 |
| rs749943648 | snp | C/T | 3.97875e-05 | 0.00446007 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017441 | CTCCAGAAAAGGGCC[C/T]CCGTCGTCTGCCCTG | 79058 |
| rs749952943 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995766 | GACCAGGCTGGGGGA[A/G]ACACGGTCAGGCATG | 79058 |
| rs749955480 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985200 | CATGCACACATCCAC[A/G]CACATACCTGCACAC | 79058 |
| rs749958842 | snp | G/T | 1.66294e-05 | 0.00288347 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012210 | GGTGCTTCCTAACAC[G/T]TAGGTGCCTTCTCTC | 79058 |
| rs749978830 | snp | C/G | 1.68892e-05 | 0.00290591 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009064 | GAGCCCGTGGACCGG[C/G]AGCCGGTGGTGTGCC | 79058 |
| rs750009111 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011256 | CAGCAGCCCAAGGTC[A/G]CAGGGGCCTCCCCCA | 79058 |
| rs750010043 | snp | A/G | 1.68826e-05 | 0.00290534 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016977 | GTCCCCTTCCCCATT[A/G]CCAGCCCCTGACCCT | 79058 |
| rs750020079 | snp | A/G | 4.71731e-05 | 0.00485637 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012142 | CCCACTTGAGGCGTC[A/G]CCCCCATCTGCAGGC | 79058 |
| rs750048353 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003592 | CTCTGGGTGGGATTC[A/G]AGGCCTGATGCCTCT | 79058 |
| rs750104672 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978915 | TGTGCCAGGAAGATG[C/T]CCGTGTTGCTGTACT | 79058 |
| rs750154220 | in-del | -/A | 0.00292112 | 0.0381055 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996106 | GGAGTCTATTTAGCT[-/A]AAAAAAAAAGTGGTC | 79058 |
| rs750160722 | snp | C/T | 1.66228e-05 | 0.0028829 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985596 | GCTTCTCAGCCATTT[C/T]CCACAGATCAGGTGA | 79058 |
| rs750209131 | in-del | -/GTGGACCGGGAGCCG | 0.00012181 | 0.00780322 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009054 | GTGGACCGGGAGCCC[-/GTGGACCGGGAGCCG]GTGGACCGGGAGCCG | 79058 |
| rs750276687 | snp | C/G | 1.72794e-05 | 0.00293928 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996508 | GCAGCCGCCAGCGCT[C/G]CACTTCCCTTGGAAT | 79058 |
| rs750280502 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000841 | GTCTTTGAAGTGCCT[C/T]CACTGGCTGGGAGGC | 79058 |
| rs750328029 | snp | G/T | 1.66632e-05 | 0.0028864 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010761 | CTGGTCCCTGGTGCA[G/T]CTCCGGCCGTCCCTC | 79058 |
| rs750455964 | snp | C/T | 0.000418848 | 0.0144654 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977769 | GCCGCCCGCCCGGGG[C/T]GGACGGGTAGGCGGG | 79058 |
| rs750468946 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988929 | ATTTCATTTCCAGGC[C/T]GGGCATGGCGGCTCT | 79058 |
| rs750491850 | snp | C/G | 1.8186e-05 | 0.0030154 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015118 | TCACCCTGGGTCCCT[C/G]GCTGAAACGGTGCCT | 79058 |
| rs750499412 | snp | A/G | 6.61179e-05 | 0.00574931 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009564 | GCTGGAGCGCTACCC[A/G]AAGGTCTGCAGACAG | 79058 |
| rs750525475 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000490 | GGCCCGGGGCCACAT[A/G]CCGCTGCTGGGTCCC | 79058 |
| rs750545230 | snp | A/G | 3.35773e-05 | 0.00409726 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017258 | GGTGGGCGGGTGGCC[A/G]GGTGGTGAGAGCCCG | 79058 |
| rs750575047 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983068 | AGGCTTGTCTCAAAC[G/T]CCTGAACCTCAGGTG | 79058 |
| rs750577038 | in-del | -/CTC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006941 | TTCCTGGCCCCTCTT[-/CTC]TGTGGGACAGAAAGT | 79058 |
| rs750704780 | snp | G/T | 1.89554e-05 | 0.00307853 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994938 | CCCACTTTCCAACTG[G/T]AAAATCTGCTGTCCC | 79058 |
| rs750768559 | snp | A/C | 1.69798e-05 | 0.00291369 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996769 | AAGCCAAAGAAGTCC[A/C]AGTCGGGCCAGGATC | 79058 |
| rs750787852 | snp | A/G/T | 3.32515e-05 | 0.00407736 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011610 | ATTTTACCTGTGTAC[A/G/T]TTTTTTCTCCTGAGC | 79058 |
| rs750814383 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993584 | ACAGTGGACCCCTGC[A/G]GCCCTGTAAGCACAC | 79058 |
| rs750815322 | snp | A/G | 5.31561e-05 | 0.00515512 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983689 | TCGTGCTCTGGGGGA[A/G]GCTGACTGTGTGGGG | 79058 |
| rs750832949 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992571 | TGGCCTCATGACCAT[C/T]TCCGGACCCCTGGCC | 79058 |
| rs750872833 | in-del | -/G | 0.000118811 | 0.00770659 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010898 | GGGGTGTCCGGGGAT[-/G]GGGGGCAGGGGCCCA | 79058 |
| rs750884143 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013607 | GCAGAGCCCCACTCC[A/G]GCTGCCTGCTGCCTG | 79058 |
| rs750939425 | in-del | -/G | | | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009620 | CTGAGGGGGCCCCCC[-/G]GTGAGGTCTGTGGAC | 79058 |
| rs750960553 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982869 | CCCAGGCAGGAGTGC[A/G]GTGGCATGATCTTGC | 79058 |
| rs750966096 | in-del | -/TG | 0.0102421 | 0.0708249 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010091 | AATTTTTGTTGTTTT[-/TG]TTTTTTTTTTACTAG | 79058 |
| rs750999958 | snp | C/G/T | 7.50034e-05 | 0.00612348 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012138 | CTGCCCCACTTGAGG[C/G/T]GTCACCCCCATCTGC | 79058 |
| rs751099966 | snp | C/G | 3.33751e-05 | 0.0040849 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011629 | TTTCTCCTGAGCCCA[C/G]TCCTGCCTCCAGTGC | 79058 |
| rs751150467 | snp | A/G | 1.70653e-05 | 0.00292102 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016828 | GCCTGGCCTGCTGGA[A/G]CATGCCATCTCCCCA | 79058 |
| rs751167717 | in-del | -/T | 1.7161e-05 | 0.0029292 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009583 | TCTGCAGACAGGATG[-/T]TGGGGGCGACTGAGG | 79058 |
| rs751219769 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992089 | GTGTGCCAGTACCCT[C/G]CTGCGAGCAGGCACC | 79058 |
| rs751219833 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005839 | AGCTCCAGCCCCAGC[A/G]TGACCGTGTGTGTGG | 79058 |
| rs751229878 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013459 | GCCTCGGGGCCTCTC[A/G]GGGTGGTGTCCCCGG | 79058 |
| rs751233400 | snp | A/C | 1.68975e-05 | 0.00290662 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985460 | GGATTTAGAAGGAAT[A/C]GTTGCTTTTCTTCCT | 79058 |
| rs751288850 | snp | C/T | 3.55524e-05 | 0.00421603 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996438 | TGTCATGAAGTGCTA[C/T]GACCCCGTGGGCAAG | 79058 |
| rs751290352 | snp | A/G | 3.46422e-05 | 0.00416172 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996499 | GCTGGCCAGGCAGCC[A/G]CCAGCGCTCCACTTC | 79058 |
| rs751357539 | snp | C/T | 4.04654e-05 | 0.00449789 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996117 | AGCTAAAAAAAAAAG[C/T]GGTCTCAAAGGAAAG | 79058 |
| rs751377065 | snp | C/G | 0.000163572 | 0.00904209 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010072 | CCGCTACCACTAGCT[C/G]GGCTAATTTTTGTTG | 79058 |
| rs751410953 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981152 | TGAAGAAACCGCAAG[A/G]GAGAAGGGCCTGGCG | 79058 |
| rs751430083 | snp | A/G | 6.29941e-05 | 0.00561187 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009552 | GATAAAGGAGAAGCT[A/G]GAGCGCTACCCAAAG | 79058 |
| rs751487139 | snp | G/T | 1.95189e-05 | 0.00312395 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015093 | CAGCTTGGTGACCGG[G/T]TGGCTCCATTCACCC | 79058 |
| rs751526833 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986068 | CTCAGCCTCCCAAAG[C/T]GTTGAGATTACAGGT | 79058 |
| rs751586724 | snp | C/T | 3.62384e-05 | 0.00425651 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994924 | CCGCTCACTTTCAGC[C/T]CACTTTCCAACTGGA | 79058 |
| rs751590996 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979206 | AGGACACGTGCCGGC[A/G]GCAGGACTTCAACCC | 79058 |
| rs751639894 | snp | A/G | 3.33428e-05 | 0.00408293 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994841 | GCCTGCAGCACCCCG[A/G]CGGGGCCACCCCAGT | 79058 |
| rs751641748 | snp | C/T | 1.69026e-05 | 0.00290706 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996751 | AGCCCTGGAGGCCCC[C/T]CCAAGCCAAAGAAGT | 79058 |
| rs751642969 | snp | G/T | 1.96408e-05 | 0.00313369 | missense, nc-transcript-variant, splice-donor-variant | ASPSCR1 | GRCh38.p7 | 17:82017089 | AGGAGCCTGGGCAAG[G/T]TGCCCAAGTGGCTGA | 79058 |
| rs751687437 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008240 | TGGGTGGGAGACTGC[A/G]GGGTAGACGGGACGG | 79058 |
| rs751717850 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989924 | ACCTGAGTAGCTGGG[A/T]TTACTGGCGCACGCC | 79058 |
| rs751751044 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979941 | TGTCTATCCCACACG[C/T]GAAGCTTTTCACTTT | 79058 |
| rs751786019 | snp | C/T | 3.34052e-05 | 0.00408674 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011531 | TCTGTATGTTCTTTT[C/T]CTCCTCTGCAGTGGG | 79058 |
| rs751826005 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985824 | CATCGTTCTGAGTTT[A/C]CTGGGCCCAGCGGCC | 79058 |
| rs751897755 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007392 | GAAGTCAACAGCCCC[A/C]TAGCAGCGTGATGCT | 79058 |
| rs751899446 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014743 | CTACAGAGTTGCTGC[C/T]CCGTGGGGGTTGACG | 79058 |
| rs751920088 | snp | A/G | 5.0822e-05 | 0.00504068 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010892 | CGCTGTGGGGTGTCC[A/G]GGGATGGGGGGCAGG | 79058 |
| rs751926686 | snp | A/G | 1.79371e-05 | 0.0029947 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983630 | GCCAAGCTGGAGATG[A/G]TGCCCGCTTCCCGGA | 79058 |
| rs751939572 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005546 | CCCAGGGACACCTGG[C/T]GGCCACACACCTGGG | 79058 |
| rs751959040 | snp | A/G | 4.39831e-05 | 0.00468931 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996069 | CGCCACCATCAGGTA[A/G]GGGCAGTGCTGCTGG | 79058 |
| rs751969775 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985103 | ACATCTGCGCACATA[C/G]CCGCACACACCTGCA | 79058 |
| rs751981825 | snp | A/G | 6.38237e-05 | 0.0056487 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983559 | TGTCTTGCAGGTTTC[A/G]GAGGAGCGTGCTCGA | 79058 |
| rs751991425 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013665 | TTCCGAGAGGGACAG[C/T]GTGCGTGGGTGTGGG | 79058 |
| rs752020640 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983167 | TTTTCTGTGGTGGCT[C/T]CAGCCGTGACGGCCG | 79058 |
| rs752066409 | snp | A/G | 6.57124e-05 | 0.00573166 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996014 | GTGAAGCTGCCCTGC[A/G]GGGCACGACGCTGCA | 79058 |
| rs752139912 | snp | G/T | 1.73366e-05 | 0.00294415 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016818 | TCTACCTGGAGCCTG[G/T]CCTGCTGGAGCATGC | 79058 |
| rs752154481 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006022 | CTGTGGTTTTCTTTT[C/G]TGTGCATGTCCATGC | 79058 |
| rs752189217 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976655 | AGGCTACTGGGCAGC[C/T]GAGCCCTAGCCAGGA | 79058 |
| rs752288139 | in-del | -/CGGGTGGAGGG | 2.44114e-05 | 0.00349358 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017149 | GTGGGGTGCTGTGGC[-/CGGGTGGAGGG]CGGGGGTCCGGGTGC | 79058 |
| rs752297999 | snp | A/G | 9.9686e-05 | 0.00705925 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016523 | GGGAGCCGAGGAGCC[A/G]GCAGGTGAGTGTCAG | 79058 |
| rs752399655 | snp | C/T | 1.7509e-05 | 0.00295875 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009435 | CCCGGGGCCTGTTGC[C/T]AGGGCCCCCATTCTG | 79058 |
| rs752402535 | snp | A/G | 2.71433e-05 | 0.00368387 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996094 | TGCTGGGGCCGAGGA[A/G]TCTATTTAGCTAAAA | 79058 |
| rs752437701 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993884 | GCATGACCTGAGGCC[A/G]GCCCTGGCCTCCCCT | 79058 |
| rs752447248 | snp | A/G/T | 6.18295e-05 | 0.00555976 | synonymous-codon, missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009537 | CTTCAGGGAGGCGCA[A/G/T]ATAAAGGAGAAGCTG | 79058 |
| rs752452776 | snp | C/G | 1.67069e-05 | 0.00289019 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012325 | GCGGGGCGGGGCCCT[C/G]CAGGGAGGGCAGGAC | 79058 |
| rs752471492 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987054 | CGGGCAGGGGTGAGC[A/G]GGACCCGAGGCAGGA | 79058 |
| rs752508603 | snp | A/G | 2.06951e-05 | 0.0032167 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015085 | TCCAGCCCCAGCTTG[A/G]TGACCGGGTGGCTCC | 79058 |
| rs752549373 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999029 | TTGTCCCTGTCCTGA[C/T]CCCGCATCAGAGCCC | 79058 |
| rs752611634 | snp | C/G | 3.8301e-05 | 0.00437596 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017079 | GCCCGTGAAGAGGAG[C/G]CTGGGCAAGGTGCCC | 79058 |
| rs752616825 | snp | A/C | 1.66018e-05 | 0.00288108 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012250 | CACCCCTCCAAAAAC[A/C]GTCCTGGACGACCAC | 79058 |
| rs752745576 | snp | A/C | 3.334e-05 | 0.00408276 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994837 | GAGTGCCTGCAGCAC[A/C]CCGGCGGGGCCACCC | 79058 |
| rs752748823 | snp | A/C | 1.71311e-05 | 0.00292664 | stop-gained, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996588 | CTCAGGGCCCTGCTG[A/C]GAGCACACTCAGGAG | 79058 |
| rs752772681 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981343 | AGGCTGGTTCAGTTG[C/G]TTGGGGGGGGCTTAG | 79058 |
| rs752796536 | snp | C/G/T | 6.74302e-05 | 0.00580613 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996655 | GTTCCTTTCTCGGGT[C/G/T]GGGGACAGAGACTGG | 79058 |
| rs752803131 | snp | A/T | 1.68052e-05 | 0.00289867 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010880 | ACAGGTGGGCAGCGC[A/T]GTGGGGTGTCCGGGG | 79058 |
| rs752807625 | snp | A/G | 1.70831e-05 | 0.00292254 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017014 | AAGTCTGAGCCAGCT[A/G]CTGAGGAGGGGGCGC | 79058 |
| rs752825619 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980083 | CACCTCCTAGGTTCA[A/G]GTGATTCTCCTGCCT | 79058 |
| rs752860661 | snp | A/G | 1.94786e-05 | 0.00312072 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015355 | ACGTGGGGACAGGCC[A/G]GGTAGGCTGCCTGGC | 79058 |
| rs752947915 | in-del | -/C | | | upstream-variant-2KB, intron-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977016 | CCCACGGTTCTGAAA[-/C]CGGTCTCCCGCCTTT | 79058 |
| rs753005965 | snp | G/T | 2.8823e-05 | 0.00379614 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983531 | TCTGCAGGGCAGCAA[G/T]TGTGCTCTGGTCTGT | 79058 |
| rs753059133 | snp | C/T | 4.41969e-05 | 0.00470069 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996011 | CGGGTGAAGCTGCCC[C/T]GCGGGGCACGACGCT | 79058 |
| rs753059229 | snp | A/G | 1.64776e-05 | 0.00287028 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979248 | ATCTGAAGTGAGTTT[A/G]CTCCAGCTCAGCAGC | 79058 |
| rs753060617 | snp | C/T | 1.79181e-05 | 0.00299311 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015289 | CCTCCTCTCCACCAT[C/T]CCCTCGTCCGAGCAG | 79058 |
| rs753102442 | snp | C/T | 9.55648e-05 | 0.00691182 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017347 | GCCTGAGGTGCCCAC[C/T]CCGCCAGCCACAGGA | 79058 |
| rs753221410 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983207 | ACACTCCAGCTTCCG[C/T]GAGTGCAGCAGTGTT | 79058 |
| rs753287059 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004505 | ACCTGCAGGAGGAGT[C/T]GGGTCTTTCACAGCT | 79058 |
| rs753298977 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994042 | TGGGGAGTTGGAAAC[A/G]CAGAGGCAAGCCCGC | 79058 |
| rs753327169 | snp | C/T | 7.27864e-05 | 0.00603224 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996088 | CAGTGCTGCTGGGGC[C/T]GAGGAGTCTATTTAG | 79058 |
| rs753355747 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007669 | GGGCTCCTCCAGGGA[A/G]GCTCTGGACCAGGCT | 79058 |
| rs753380156 | snp | A/G | 0.000164775 | 0.00907525 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009227 | TCCCGGCATCTTCGC[A/G]CCAGGGTTTGCCCCA | 79058 |
| rs753383888 | snp | A/G | 4.49196e-05 | 0.00473896 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015387 | CAGTGCTCCCTGCAC[A/G]GAGGCGCAGACAGGG | 79058 |
| rs753456785 | in-del | -/CC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985043 | ACATGCACACACCTC[-/CC]CCCCCCACACACACC | 79058 |
| rs753524502 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995867 | GCCAGATGTGGGGGG[-/T]GGGTAGGATGGAGGC | 79058 |
| rs753548503 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000483 | CGCAGAGGGCCCGGG[A/G]CCACATGCCGCTGCT | 79058 |
| rs753573141 | snp | C/G | 1.66043e-05 | 0.00288129 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012235 | TCTCTCCTCAGTCAT[C/G]ACCCCTCCAAAAACA | 79058 |
| rs753624182 | snp | G/T | 1.69318e-05 | 0.00290957 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016992 | GCCAGCCCCTGACCC[G/T]GCACCTAAGTCTGAG | 79058 |
| rs753685368 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989680 | TGGATGGACACTGCC[A/G]CGTGTTTGAAACGTT | 79058 |
| rs753691563 | snp | A/G | 1.67033e-05 | 0.00288987 | splice-donor-variant | ASPSCR1 | GRCh38.p7 | 17:81985608 | TTTTCCACAGATCAG[A/G]TGAGCATCAGTGGGC | 79058 |
| rs753724293 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997038 | AGGAATTTAGGGGTA[A/G]GCAGGTGGTAGAGAA | 79058 |
| rs753738478 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988776 | GTGGGTGTTGCGGGG[C/G]ATCTGGCTGTGTCTC | 79058 |
| rs753768899 | in-del | -/CAGGACTCTTTCTGTT | 1.6577e-05 | 0.00287893 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985546 | GATGGCTCGAGGTTG[-/CAGGACTCTTTCTGTT]CAGGCCAGACCCTCT | 79058 |
| rs753769333 | snp | C/T | 1.67725e-05 | 0.00289585 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016930 | CACTCTGTGTCTTCG[C/T]CTCCCCACAGGTACA | 79058 |
| rs753874676 | snp | C/G | 1.71449e-05 | 0.00292782 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996582 | GGACACCTCAGGGCC[C/G]TGCTGCGAGCACACT | 79058 |
| rs753877158 | snp | A/G | 1.64751e-05 | 0.00287007 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979226 | GACTTCAACCCCTGT[A/G]AATATGATCTGAAGT | 79058 |
| rs753889623 | snp | C/T | 1.6659e-05 | 0.00288604 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010769 | TGGTGCAGCTCCGGC[C/T]GTCCCTCCAACCCTT | 79058 |
| rs753927778 | snp | A/G | 8.32092e-05 | 0.00644963 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010830 | TCCTGTTCCCCGACC[A/G]CTACGTCCTACAGGG | 79058 |
| rs753951804 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999154 | GACTGGGGGACTGTC[A/G]TGCGGCTTTCGGTGA | 79058 |
| rs753988931 | snp | A/C/G | 7.05647e-05 | 0.00593955 | downstream-variant-500B, intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017416 | CCTCAACGCCTTCCT[A/C/G]TCATGCTTCCTCCAG | 79058 |
| rs753990353 | snp | C/G | 5.36687e-05 | 0.00517991 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015197 | CGTGGACTCTGGGAG[C/G]CTTCTTTTTTGGGGT | 79058 |
| rs754072647 | snp | A/G | 5.576e-05 | 0.00527986 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995949 | TCCCTGGGCTCTGGG[A/G]TCCCGGTGCAAGGCG | 79058 |
| rs754164537 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004794 | TCGGGAAGAAGGGAG[C/T]GTGGGGCCTTTGGAA | 79058 |
| rs754239673 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010628 | GGCACTTGGCTGTCT[-/C]CATGCCCAGCCTGCC | 79058 |
| rs754289572 | snp | G/T | 1.65751e-05 | 0.00287876 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996876 | AGGCCTTGGGACTTG[G/T]GGGTGTCCTTTCTCC | 79058 |
| rs754342953 | snp | C/G | 1.6651e-05 | 0.00288535 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011619 | GTGTACGTTTTTTCT[C/G]CTGAGCCCACTCCTG | 79058 |
| rs754369693 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981413 | AGGTGGAGTCTCGCT[C/T]TGTCACACAGGCTGT | 79058 |
| rs754382108 | snp | C/T | 3.32044e-05 | 0.00407444 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985504 | ATGTCTTATACCCTC[C/T]AGGTTCGCATCGCTT | 79058 |
| rs754454543 | in-del | -/C | 2.17323e-05 | 0.00329631 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009609 | GAGGCACAGCTCTGA[-/C]GGGGGCCCCCCGTGA | 79058 |
| rs754464527 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996668 | GTGGGGGACAGAGAC[-/T]GGGGGGCCCTCCTGG | 79058 |
| rs754479763 | snp | C/T | 4.67607e-05 | 0.00483509 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015392 | CTCCCTGCACAGAGG[C/T]GCAGACAGGGAGCCC | 79058 |
| rs754525845 | snp | A/G | 0.000172344 | 0.00928128 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996089 | AGTGCTGCTGGGGCC[A/G]AGGAGTCTATTTAGC | 79058 |
| rs754551173 | in-del | -/T | 1.67511e-05 | 0.00289401 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996104 | AGGAGTCTATTTAGC[-/T]TAAAAAAAAAAGTGG | 79058 |
| rs754576803 | snp | A/G | 1.65318e-05 | 0.002875 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996021 | TGCCCTGCGGGGCAC[A/G]ACGCTGCAGTCGCTG | 79058 |
| rs754579521 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981579 | GGACGGGGTTTCACC[A/G]TGTTGGTCATGCTGG | 79058 |
| rs754580874 | snp | A/G | 3.26824e-05 | 0.00404229 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009230 | CGGCATCTTCGCGCC[A/G]GGGTTTGCCCCATCG | 79058 |
| rs754581751 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985173 | GCACACCTGCACACA[-/C]CCACACACCAACATG | 79058 |
| rs754633997 | snp | C/T | 2.21919e-05 | 0.00333098 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009173 | TGAGAAGACGCTTGG[C/T]CCAGCTCAAGAGTGA | 79058 |
| rs754647845 | in-del | -/TG | 0.00423428 | 0.0458171 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010089 | CTAATTTTTGTTGTT[-/TG]TTTTTTTTTTTTACT | 79058 |
| rs754675985 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994492 | GAGCCAGTGCTGCTC[A/G]CCCCTCCTGTGCGGT | 79058 |
| rs754700719 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005862 | GTGTGTGGGAAAACC[A/G]TCCGGGTACTTGGGG | 79058 |
| rs754713092 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013489 | GTGACGTGCCTGCCT[C/G]CCTGCCTGCCGTCAG | 79058 |
| rs754779975 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996350 | CGGGAGAGGGTGAGC[C/T]TGGGCCGGGAGAGGG | 79058 |
| rs754862623 | snp | A/C | 1.66037e-05 | 0.00288125 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012237 | TCTCCTCAGTCATCA[A/C]CCCTCCAAAAACAGT | 79058 |
| rs754867448 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979474 | TCTGTGGCTTGTGGC[C/T]GCATTGCTCTCTGCC | 79058 |
| rs754887850 | snp | A/T | 1.71361e-05 | 0.00292707 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996583 | GACACCTCAGGGCCC[A/T]GCTGCGAGCACACTC | 79058 |
| rs754892182 | snp | C/G | 0.000251587 | 0.0112129 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016933 | TCTGTGTCTTCGCCT[C/G]CCCACAGGTACATGT | 79058 |
| rs754909708 | snp | C/T | 3.4053e-05 | 0.00412618 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017008 | GCACCTAAGTCTGAG[C/T]CAGCTGCTGAGGAGG | 79058 |
| rs754946078 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986111 | GCCCCACCAGAAAAT[C/T]TTCCTAATAGTAATT | 79058 |
| rs754979623 | snp | A/G | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985523 | TTCGCATCGCTTTGC[A/G]GCTGGACGATGGCTC | 79058 |
| rs754990425 | snp | C/G | | | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977464 | GACCGCGCTTTCCGG[C/G]TCTGGCGCGGGCTTT | 79058 |
| rs755155984 | snp | C/T | 5.17951e-05 | 0.0050887 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996538 | TCTGGGGAGCTCAGC[C/T]GCGGCGACTTGAGCC | 79058 |
| rs755159815 | snp | A/G | 1.64757e-05 | 0.00287012 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979239 | GTGAATATGATCTGA[A/G]GTGAGTTTGCTCCAG | 79058 |
| rs755208805 | snp | A/G/T | 9.99341e-05 | 0.0070681 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010770 | GGTGCAGCTCCGGCC[A/G/T]TCCCTCCAACCCTTC | 79058 |
| rs755221600 | snp | C/T | 1.78896e-05 | 0.00299073 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015199 | TGGACTCTGGGAGGC[C/T]TCTTTTTTGGGGTCC | 79058 |
| rs755230363 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005612 | CCTGCACTGCTGAGG[-/T]TTGGGCCTCATTCCC | 79058 |
| rs755245732 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008249 | GACTGCAGGGTAGAC[A/G]GGACGGGACCAGGAG | 79058 |
| rs755283613 | snp | A/G | 1.64876e-05 | 0.00287116 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979146 | GCCCGCCAGCCCTGC[A/G]CACTCAGCAGTTCAC | 79058 |
| rs755336724 | snp | A/G | 0.000107129 | 0.00731801 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995015 | ACGACGTGTTTCATG[A/G]AAAAAGAGGGAGTGG | 79058 |
| rs755380107 | snp | C/G/T | 0.000194991 | 0.00987224 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995953 | TGGGCTCTGGGGTCC[C/G/T]GGTGCAAGGCGCACC | 79058 |
| rs755490680 | snp | A/G | 1.88276e-05 | 0.00306813 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996877 | GGCCTTGGGACTTGG[A/G]GGTGTCCTTTCTCCT | 79058 |
| rs755510254 | snp | C/T | 1.66554e-05 | 0.00288573 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011620 | TGTACGTTTTTTCTC[C/T]TGAGCCCACTCCTGC | 79058 |
| rs755548911 | snp | A/G | 1.72493e-05 | 0.00293672 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996789 | GGGCCAGGATCCCCA[A/G]CAGGAGCAGGAGCAG | 79058 |
| rs755570961 | in-del | -/C | 1.66604e-05 | 0.00288616 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010768 | CTGGTGCAGCTCCGG[-/C]CGTCCCTCCAACCCT | 79058 |
| rs755626901 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006629 | TGGCCTGCACAGGCA[G/T]CCCGTTTCTTTTCTC | 79058 |
| rs755649427 | snp | A/G | 0.000107216 | 0.00732095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995964 | GTCCCGGTGCAAGGC[A/G]CACCTGTCCTGGCTG | 79058 |
| rs755699918 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992615 | TGGGGAGCGGGGACC[C/T]TGGGCCCTCCCTGTC | 79058 |
| rs755751868 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993939 | CCCTCCTCTCGGATT[C/T]CCCTCCCTGGAGAGG | 79058 |
| rs755811881 | in-del | -/TCTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982748 | TTCTTGTTTTCTCTT[-/TCTT]TCTTTCTTTCTTTCT | 79058 |
| rs755867505 | snp | A/G | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017624 | AACAGAAGTGCTTGA[A/G]GAAAGTCTTTTGGGG | 79058 |
| rs755996784 | snp | A/C/G | 8.38657e-05 | 0.00647508 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016929 | CCACTCTGTGTCTTC[A/C/G]CCTCCCCACAGGTAC | 79058 |
| rs756018211 | snp | A/G | 1.65844e-05 | 0.00287957 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985516 | CTCCAGGTTCGCATC[A/G]CTTTGCAGCTGGACG | 79058 |
| rs756060215 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976659 | TACTGGGCAGCTGAG[C/G]CCTAGCCAGGAGTCC | 79058 |
| rs756067586 | snp | C/T | 1.72662e-05 | 0.00293817 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996515 | CCAGCGCTCCACTTC[C/T]CTTGGAATCTGGGGA | 79058 |
| rs756076506 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006028 | TTTTCTTTTGTGTGC[A/G]TGTCCATGCTTGGGT | 79058 |
| rs756237541 | snp | C/G | 0.000606428 | 0.0174025 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977774 | CCGCCCGGGGCGGAC[C/G]GGTAGGCGGGCGGGG | 79058 |
| rs756275622 | snp | G/T | 1.68026e-05 | 0.00289845 | splice-donor-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009569 | AGCGCTACCCAAAGG[G/T]CTGCAGACAGGATGT | 79058 |
| rs756292623 | snp | A/G | 2.07196e-05 | 0.0032186 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977630 | GCCGGCCCGGCGGCG[A/G]GTCACGTGAGCGGAA | 79058 |
| rs756308454 | snp | C/G | 2.08088e-05 | 0.00322552 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994949 | ACTGGAAAATCTGCT[C/G]TCCCGCAGCCGTCTC | 79058 |
| rs756320525 | snp | A/G | 0.000145201 | 0.00851936 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995005 | TCTTGAAAGCACGAC[A/G]TGTTTCATGGAAAAA | 79058 |
| rs756328516 | snp | A/G | 1.81427e-05 | 0.00301182 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015119 | CACCCTGGGTCCCTC[A/G]CTGAAACGGTGCCTG | 79058 |
| rs756349959 | snp | A/G | 1.67877e-05 | 0.00289716 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017262 | GGCGGGTGGCCGGGT[A/G]GTGAGAGCCCGGGGT | 79058 |
| rs756356226 | in-del | -/AG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994377 | TCAGGCGGTGGAGAC[-/AG]GGGCACCTCCTCTTA | 79058 |
| rs756413641 | snp | C/T | 6.43646e-05 | 0.00567258 | missense, nc-transcript-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017111 | AGTGGCTGAAGCTGC[C/T]GGGTACTGCGGCTGG | 79058 |
| rs756426183 | snp | A/G | 8.62121e-05 | 0.00656495 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996558 | CGACTTGAGCCGTCC[A/G]GAGGACGCGGACACC | 79058 |
| rs756426253 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012050 | GGCCTGCCCCCCACC[A/G]GCCCTTCCGAGCCCT | 79058 |
| rs756459935 | in-del | -/AGA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003436 | CTGGGCAACAGAGCG[-/AGA]CGCTGTCTCAAAACA | 79058 |
| rs756493385 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989975 | GTATTTTTTTTAGTA[C/G]AGACAGGGTTTCACC | 79058 |
| rs756502959 | snp | A/G | 1.69899e-05 | 0.00291456 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996771 | GCCAAAGAAGTCCAA[A/G]TCGGGCCAGGATCCC | 79058 |
| rs756599249 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986211 | GGCGAATCGCTTGAG[C/T]TCATGAGTTCAAGAC | 79058 |
| rs756601470 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980149 | CAACACACCCAGCTA[A/G]TTTTTATATTTTTAG | 79058 |
| rs756622860 | snp | A/C | 1.64765e-05 | 0.00287019 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996687 | GGGCCCTCCTGGGCC[A/C]ACGAGGCCTCTGACA | 79058 |
| rs756642599 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990955 | TGAATCCCACGTCCC[A/G]TAAGGACCTAGTTGC | 79058 |
| rs756669382 | snp | C/G | 1.66696e-05 | 0.00288696 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011537 | TGTTCTTTTTCTCCT[C/G]TGCAGTGGGGGACTT | 79058 |
| rs756718621 | snp | C/T | 2.15343e-05 | 0.00328126 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016514 | GGTGCACTTGGGAGC[C/T]GAGGAGCCGGCAGGT | 79058 |
| rs756720633 | snp | C/G/T | 3.4676e-05 | 0.00416378 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010918 | GCAGGGGCCCATGGG[C/G/T]CCTCTCCCGGCTCCT | 79058 |
| rs756745360 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988149 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 79058 |
| rs756788805 | in-del | -/AT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984616 | AACATTTACCATCTC[-/AT]ATGTGGCTTCTGAGG | 79058 |
| rs756807994 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983217 | TTCCGCGAGTGCAGC[A/G]GTGTTCACGCCCCAG | 79058 |
| rs756835393 | snp | C/T | 1.66963e-05 | 0.00288927 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011632 | CTCCTGAGCCCACTC[C/T]TGCCTCCAGTGCTCG | 79058 |
| rs756872308 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014898 | CCTCAGGCTGTGTCA[A/G]GGCAGGGCGGGCACC | 79058 |
| rs756986856 | snp | C/T | 5.19036e-05 | 0.00509402 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996504 | CCAGGCAGCCGCCAG[C/T]GCTCCACTTCCCTTG | 79058 |
| rs757009494 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976756 | GGGGCGGAACACGTG[C/T]GAGTGCTGTCCATGA | 79058 |
| rs757059664 | snp | C/T | 3.37672e-05 | 0.00410883 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985465 | TAGAAGGAATAGTTG[C/T]TTTTCTTCCTAAGGA | 79058 |
| rs757114856 | snp | A/G | 1.76958e-05 | 0.00297449 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996439 | GTCATGAAGTGCTAC[A/G]ACCCCGTGGGCAAGA | 79058 |
| rs757120734 | in-del | -/GAGCACAAAAGTGGTTT | 2.6454e-05 | 0.0036368 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994969 | CAGCCGTCTCCAGGG[-/GAGCACAAAAGTGGTTT]CAGTGGCGGGAGACT | 79058 |
| rs757179308 | snp | C/T | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017755 | CCTGCTGCCCCCGAG[C/T]GGGCTATAGTGCTGG | 79058 |
| rs757181246 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997170 | ATGACAAGGCGGCAA[C/G]TGTGTCAGCTCCGTG | 79058 |
| rs757204167 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006868 | GCTCACCAGTCAACA[A/G]GGCTGGGTGTGGCTG | 79058 |
| rs757210501 | snp | A/C/T | 6.37125e-05 | 0.00564378 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009556 | AAGGAGAAGCTGGAG[A/C/T]GCTACCCAAAGGTCT | 79058 |
| rs757265896 | snp | G/T | 1.92558e-05 | 0.00310282 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015096 | CTTGGTGACCGGGTG[G/T]CTCCATTCACCCTGG | 79058 |
| rs757339449 | snp | A/G | 2.40399e-05 | 0.0034669 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017162 | GCCGGGTGGAGGGCG[A/G]GGGTCCGGGTGCTGT | 79058 |
| rs757370849 | snp | A/G | 1.82344e-05 | 0.00301941 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994926 | GCTCACTTTCAGCCC[A/G]CTTTCCAACTGGAAA | 79058 |
| rs757428130 | snp | C/T | 0.000183454 | 0.00957567 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994842 | CCTGCAGCACCCCGG[C/T]GGGGCCACCCCAGTC | 79058 |
| rs757459426 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999157 | TGGGGGACTGTCATG[C/T]GGCTTTCGGTGACAG | 79058 |
| rs757483369 | snp | A/G | 3.35672e-05 | 0.00409664 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996669 | TGGGGGACAGAGACT[A/G]GGGGGCCCTCCTGGG | 79058 |
| rs757492967 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975888 | CCTGCCTCAGCCTCC[C/T]AAATATTTAATAACT | 79058 |
| rs757526444 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000463 | CCATCGCCGCCAGCC[A/G]CACACGCAGAGGGCC | 79058 |
| rs757596721 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987324 | AGAAGCAGGGATCCC[A/G]GCGCCCTGGCTCTGT | 79058 |
| rs757613960 | snp | G/T | 7.20747e-05 | 0.00600268 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983632 | CAAGCTGGAGATGGT[G/T]CCCGCTTCCCGGAGC | 79058 |
| rs757628185 | snp | G/T | 3.40518e-05 | 0.00412611 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010903 | GTCCGGGGATGGGGG[G/T]CAGGGGCCCATGGGG | 79058 |
| rs757683241 | snp | A/C | 2.14691e-05 | 0.00327629 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015380 | CCTGGCTCAGTGCTC[A/C]CTGCACAGAGGCGCA | 79058 |
| rs757687384 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982275 | CGCCCAGCGCATTGT[C/T]ACTTCTCAGTGTTCA | 79058 |
| rs757697470 | snp | C/G | 3.32591e-05 | 0.0040778 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012287 | ACCCTCTTTCAGGTA[C/G]CTGAGGGCCTCCCTG | 79058 |
| rs757739542 | in-del | -/TT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009916 | ATTTAGAATGAAACC[-/TT]TTTTTTTTTTTGAGA | 79058 |
| rs757747146 | snp | A/G | 2.02776e-05 | 0.00318408 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983565 | GCAGGTTTCAGAGGA[A/G]CGTGCTCGACCTTTC | 79058 |
| rs757798466 | snp | G/T | 8.72753e-05 | 0.0066053 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996015 | TGAAGCTGCCCTGCG[G/T]GGCACGACGCTGCAG | 79058 |
| rs757811154 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988836 | TGTGCAGCTGGAGGC[A/C]TTTGCACCTGGTCAC | 79058 |
| rs757818825 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981439 | GCTGTAGTACAGTGG[C/T]GCTATCTCGGCTCAC | 79058 |
| rs757913390 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985835 | GTTTCCTGGGCCCAG[C/T]GGCCCAGCCTTGCCC | 79058 |
| rs757918285 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991080 | TGGAACGATGCCAAG[A/G]GTGAGCCGTGGGAAC | 79058 |
| rs757944752 | snp | C/G | 9.08752e-05 | 0.00674013 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996417 | TCCTCTGGCCCCACT[C/G]AGGTTTGTCATGAAG | 79058 |
| rs757952986 | snp | A/G | 4.46249e-05 | 0.0047234 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016526 | AGCCGAGGAGCCGGC[A/G]GGTGAGTGTCAGTGG | 79058 |
| rs757980343 | snp | G/T | 1.72389e-05 | 0.00293584 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016821 | ACCTGGAGCCTGGCC[G/T]GCTGGAGCATGCCAT | 79058 |
| rs758004935 | snp | A/G | 1.89975e-05 | 0.00308195 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983643 | TGGTGCCCGCTTCCC[A/G]GAGCCGTGAGGGGCC | 79058 |
| rs758044279 | snp | A/G | 1.66338e-05 | 0.00288386 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011548 | TCCTCTGCAGTGGGG[A/G]ACTTGCGAGACTTCG | 79058 |
| rs758054710 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004812 | GGGGCCTTTGGAAGC[C/T]GGGCCCAGGCAGTGA | 79058 |
| rs758080316 | snp | A/G | 3.34213e-05 | 0.00408773 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996098 | GGGGCCGAGGAGTCT[A/G]TTTAGCTAAAAAAAA | 79058 |
| rs758123752 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011835 | GCCTTCTCTCTCAGC[A/G]CCCTGCTCCCCTCTG | 79058 |
| rs758144587 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003708 | AGGCAGTCCCGCCTG[C/T]GTCCTTTGTGCATGC | 79058 |
| rs758171597 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008099 | GGTCTCAGGTGTGTC[C/T]GGAGGGCAGCCCTGG | 79058 |
| rs758176191 | in-del | -/AA | 2.26442e-05 | 0.00336475 | frameshift-variant, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009181 | CGCTTGGCCCAGCTC[-/AA]GAGTGAGCGGTGGGT | 79058 |
| rs758189309 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976740 | CATGGAGGTGGGGGG[A/C]GGGGCGGAACACGTG | 79058 |
| rs758234217 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994186 | ATACCTGCCCACCCA[C/T]GCACGGGTCCAGCTG | 79058 |
| rs758249476 | snp | A/G | 2.3512e-05 | 0.00342862 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009189 | CCAGCTCAAGAGTGA[A/G]CGGTGGGTGCCCCCT | 79058 |
| rs758276491 | snp | C/T | 0.00010189 | 0.00713685 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009440 | GGCCTGTTGCCAGGG[C/T]CCCCATTCTGACCAG | 79058 |
| rs758323830 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985259 | ACACATATGCACACA[C/T]GCACGCACACCTGCA | 79058 |
| rs758383705 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999381 | CCTGTAATCCCAGCA[G/T]TTTGGGAGACCGAGG | 79058 |
| rs758392324 | snp | C/G | 1.67103e-05 | 0.00289048 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012326 | CGGGGCGGGGCCCTC[C/G]AGGGAGGGCAGGACG | 79058 |
| rs758427546 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988930 | TTTCATTTCCAGGCC[A/G]GGCATGGCGGCTCTC | 79058 |
| rs758443751 | snp | C/T | 1.91881e-05 | 0.00309737 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017080 | CCCGTGAAGAGGAGC[C/T]TGGGCAAGGTGCCCA | 79058 |
| rs758445596 | snp | C/G | 1.6601e-05 | 0.00288101 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012251 | ACCCCTCCAAAAACA[C/G]TCCTGGACGACCACA | 79058 |
| rs758490638 | snp | A/G | 1.7169e-05 | 0.00292988 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017021 | AGCCAGCTGCTGAGG[A/G]GGGGGCGCTGGTCCC | 79058 |
| rs758545012 | snp | C/T | 1.70287e-05 | 0.00291788 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985632 | AGTGGGCTGGGGGCT[C/T]TTCCCTACCCTGTTT | 79058 |
| rs758563653 | snp | A/G | 1.71223e-05 | 0.00292589 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996589 | TCAGGGCCCTGCTGC[A/G]AGCACACTCAGGAGA | 79058 |
| rs758563851 | snp | G/T | 1.68946e-05 | 0.00290638 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010889 | CAGCGCTGTGGGGTG[G/T]CCGGGGATGGGGGGC | 79058 |
| rs758621833 | snp | G/T | 1.6651e-05 | 0.00288535 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010836 | TCCCCGACCGCTACG[G/T]CCTACAGGGCTTCTT | 79058 |
| rs758638665 | in-del | -/CGGCCCAGCCT | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977391 | CCGCGCGCCCAGCCC[-/CGGCCCAGCCT]CGGCCCAGCCTGGCC | 79058 |
| rs758677505 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979130 | TGACCTGGCCCACTG[C/T]GCCCGCCAGCCCTGC | 79058 |
| rs758684425 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989850 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 79058 |
| rs758693808 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983119 | GAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCACT | 79058 |
| rs758729009 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976831 | CAGGAGGGCAGCTCC[G/T]TCTGGAAGCCTGGAG | 79058 |
| rs758754445 | in-del | -/CTTC | 1.90369e-05 | 0.00308514 | intron-variant, frameshift-variant | ASPSCR1 | GRCh38.p7 | 17:82012162 | CATCTGCAGGCCTGT[-/CTTC]CTTCGGGCGCATGGA | 79058 |
| rs758803296 | snp | A/G | 3.58892e-05 | 0.00423596 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017438 | TTCCTCCAGAAAAGG[A/G]CCCCCGTCGTCTGCC | 79058 |
| rs758827084 | snp | A/G | 2.49057e-05 | 0.00352877 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983545 | AGTGTGCTCTGGTCT[A/G]TCTTGCAGGTTTCAG | 79058 |
| rs758828739 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000575 | TTCAAAGGTACACTT[C/T]AGTAAGCAAAAAGAG | 79058 |
| rs758880157 | snp | C/T | 1.64779e-05 | 0.00287031 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979251 | TGAAGTGAGTTTGCT[C/T]CAGCTCAGCAGCAGG | 79058 |
| rs758911712 | snp | C/T | 1.7888e-05 | 0.0029906 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015206 | TGGGAGGCTTCTTTT[C/T]TGGGGTCCATCCAGA | 79058 |
| rs758930108 | snp | A/G | 2.73138e-05 | 0.00369542 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995957 | CTCTGGGGTCCCGGT[A/G]CAAGGCGCACCTGTC | 79058 |
| rs758957524 | snp | C/T | 1.69519e-05 | 0.0029113 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009061 | CGGGAGCCCGTGGAC[C/T]GGGAGCCGGTGGTGT | 79058 |
| rs758969894 | snp | C/T | 0.000117874 | 0.00767614 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017349 | CTGAGGTGCCCACTC[C/T]GCCAGCCACAGGACC | 79058 |
| rs758974348 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988018 | CAAAAATTAGCCGGG[C/T]GTGGTGGTGGGTTCC | 79058 |
| rs758987255 | snp | A/G | 6.26181e-05 | 0.0055951 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995033 | AAAGAGGGAGTGGCC[A/G]GCCCTCGGAGCCCGG | 79058 |
| rs759000075 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976564 | TCAGCAATGACTGCC[A/G]GGTGCGGTGGCTCAC | 79058 |
| rs759036666 | snp | C/T | 0.000201744 | 0.0100415 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996410 | TCCCTTGTCCTCTGG[C/T]CCCACTCAGGTTTGT | 79058 |
| rs759039349 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989416 | AGGCTCTCGTGCCTA[A/G]TGTCCCTGCACTGGC | 79058 |
| rs759107268 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014758 | CCCGTGGGGGTTGAC[A/G]TGGGCCTCCTTTCGG | 79058 |
| rs759111644 | snp | A/G | 1.66921e-05 | 0.00288891 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012318 | GGGTGCTGCGGGGCG[A/G]GGCCCTCCAGGGAGG | 79058 |
| rs759144950 | snp | A/G | 0.00152478 | 0.0275692 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977698 | TCGGTGCTGGCCCCG[A/G]ACGGCCGGCGCCACA | 79058 |
| rs759152306 | in-del | -/T | 3.49803e-05 | 0.00418198 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017040 | GGCGCTGGTCCCCCC[-/T]GAGCCCATCCCAGGG | 79058 |
| rs759166213 | snp | A/G | 0.000433922 | 0.0147232 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994971 | AGCCGTCTCCAGGGC[A/G]GTGGCGGGAGACTCG | 79058 |
| rs759176148 | snp | C/T | 4.5683e-05 | 0.00477906 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015076 | CTTTCCCTTTCCAGC[C/T]CCAGCTTGGTGACCG | 79058 |
| rs759207030 | in-del | -/TG | 0.00018543 | 0.00962708 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996668 | GTGGGGGACAGAGAC[-/TG]GGGGGCCCTCCTGGG | 79058 |
| rs759212347 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984493 | GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC | 79058 |
| rs759228146 | snp | A/G | 4.80746e-05 | 0.00490255 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017146 | AAGGTGGGGTGCTGT[A/G]GCCGGGTGGAGGGCG | 79058 |
| rs759246310 | snp | C/T | 1.72427e-05 | 0.00293616 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994897 | GGCGGCCTGCTCTTG[C/T]TCACCCAGTCCCCGC | 79058 |
| rs759294150 | snp | C/T | 5.03233e-05 | 0.00501589 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996722 | CTTCAGCTAAGTTGC[C/T]GAAGTCCCTCTCCAG | 79058 |
| rs759332915 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000095 | TCGACCCGTGTGCTC[C/T]GGGTGAGCAGGGGCT | 79058 |
| rs759434023 | in-del | -/CTCCTGCCC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001277 | GTATTGGGCCAGGGG[-/CTCCTGCCC]CTGGACCCTGACGCC | 79058 |
| rs759444439 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982050 | CTTGGCACACTGCAA[C/T]CTCCGCCTCCCGGGT | 79058 |
| rs759452274 | snp | C/T | 1.66488e-05 | 0.00288515 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994825 | TCTCCTCCCAGGGAG[C/T]GCCTGCAGCACCCCG | 79058 |
| rs759454582 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011732 | ATCTGTGGCCTCCCG[A/C]CCAGGTGCCTCCTGC | 79058 |
| rs759474919 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985408 | CTGGAGGCCAGGGCG[A/G]GGCAGTCACCCTCTC | 79058 |
| rs759475392 | snp | A/G | 3.37564e-05 | 0.00410817 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996651 | CTTTGTTCCTTTCTC[A/G]GGTGGGGGACAGAGA | 79058 |
| rs759528295 | snp | C/T | 0.000671377 | 0.0183095 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010877 | GAGACAGGTGGGCAG[C/T]GCTGTGGGGTGTCCG | 79058 |
| rs759547272 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990276 | TTGGAGCATCTCGGT[C/G]TGGGCCGGGTCCTCG | 79058 |
| rs759645906 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983151 | GCCCGGGCAGTCAGG[-/T]TTTTCTGTGGTGGCT | 79058 |
| rs759729612 | snp | C/G | 1.79056e-05 | 0.00299207 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015282 | TGCCGACCCTCCTCT[C/G]CACCATCCCCTCGTC | 79058 |
| rs759795289 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010131 | TTTACCATGTTGGCC[C/T]GGCTGGTCTCGAACT | 79058 |
| rs759962009 | snp | C/T | 2.44789e-05 | 0.00349841 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009146 | AGTTCTTTGAGCTGA[C/T]GGTGGACGACGTGAG | 79058 |
| rs759968797 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003267 | CCTGGGCAACATAAC[A/G]AGACCCCATCTCTAC | 79058 |
| rs759975282 | snp | C/T | 1.65776e-05 | 0.00287898 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985554 | GAGGTTGCAGGACTC[C/T]TTCTGTTCAGGCCAG | 79058 |
| rs759985029 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015519 | TGGGGGTCCTGGCCT[A/G]TGGGGGCTATGATGA | 79058 |
| rs760007564 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977561 | GTGCGCTGCGGCCCC[C/G]CCCCCTGGCCGCGTG | 79058 |
| rs760018468 | snp | A/G | 0.000101012 | 0.00710603 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016853 | TCCCCATCTGCGGCC[A/G]ATGTGCTGGTGGCCA | 79058 |
| rs760177814 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979731 | GTTCCCAGTGGGGCT[C/T]TGAGGGGAAAGAGCT | 79058 |
| rs760181787 | in-del | -/GAG | 1.67868e-05 | 0.00289709 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017266 | GTGGCCGGGTGGTGA[-/GAG]GAGCCCGGGGTGTGT | 79058 |
| rs760235090 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000462 | CCCATCGCCGCCAGC[C/T]GCACACGCAGAGGGC | 79058 |
| rs760243033 | snp | A/G | 1.6676e-05 | 0.00288751 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012310 | CCTCCCTGGGGTGCT[A/G]CGGGGCGGGGCCCTC | 79058 |
| rs760275278 | snp | A/C | 3.37946e-05 | 0.0041105 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016985 | CCCCATTGCCAGCCC[A/C]TGACCCTGCACCTAA | 79058 |
| rs760283296 | snp | C/G | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017608 | CACTTCCTCCAAGGA[C/G]AACAGAAGTGCTTGA | 79058 |
| rs760286696 | snp | C/T | 1.69703e-05 | 0.00291288 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994884 | GAGGGATGAGGTAGG[C/T]GGCCTGCTCTTGCTC | 79058 |
| rs760316750 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994742 | ACACCTTTGCTTTCC[A/G]AGTCTCCTGCCCCAG | 79058 |
| rs760406820 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007614 | AGTACGAGCCCATCA[G/T]GGGTACTCTGCCCGC | 79058 |
| rs760430230 | snp | A/G | 1.67217e-05 | 0.00289147 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010864 | CTTCCGCCCCAGCGA[A/G]ACAGGTGGGCAGCGC | 79058 |
| rs760477399 | snp | A/G | 1.85441e-05 | 0.00304495 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015342 | GCTGGGCACAAGCAC[A/G]TGGGGACAGGCCGGG | 79058 |
| rs760510282 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989595 | GGGGGCTGCAGGCCT[A/G]TAGCGTGCCCAGGAG | 79058 |
| rs760513440 | in-del | -/GGCCTG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994673 | GGGGCTGAGGTCTGT[-/GGCCTG]GGCCTGGGCCTGGGA | 79058 |
| rs760536415 | snp | C/T | 1.69341e-05 | 0.00290977 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996635 | CACCCGCAGCTGCCC[C/T]CTTTGTTCCTTTCTC | 79058 |
| rs760601466 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014613 | GCTGTGGTGCCGCCT[C/T]CCTCCCGGGCGTCTT | 79058 |
| rs760664436 | snp | C/T | 5.36812e-05 | 0.00518051 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015269 | ATGCCACCCAGTCTG[C/T]CGACCCTCCTCTCCA | 79058 |
| rs760681904 | in-del | -/AGCAGG | 0.000282888 | 0.0118897 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996824 | GGGAGCGGGATCCCC[-/AGCAGG]AGCAGGAGCGGGAGC | 79058 |
| rs760767593 | in-del | -/T | 1.64754e-05 | 0.00287009 | frameshift-variant, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979227 | CTTCAACCCCTGTGA[-/T]ATATGATCTGAAGTG | 79058 |
| rs760802416 | snp | A/G/T | 6.86905e-05 | 0.00586015 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81995997 | CCTCCTGCAGGTGAC[A/G/T]GGTGAAGCTGCCCTG | 79058 |
| rs760807090 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992316 | CCTGCACACTGGGCC[A/G]GCGTAGAAGGTCTGG | 79058 |
| rs760855334 | snp | C/T | 1.66186e-05 | 0.00288254 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009116 | TGCAGGCCTGGCCAG[C/T]GGAGCTGCCTGATGA | 79058 |
| rs760860327 | snp | A/G | | | intron-variant, utr-variant-5-prime | ASPSCR1 | GRCh38.p7 | 17:81982675 | CAGCTTGCATTTCCA[A/G]AGTGAGGCCAACCAC | 79058 |
| rs760863993 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992875 | GCCGTGTGTGTGGTG[C/T]GCACGTGCTCCACAG | 79058 |
| rs760969927 | snp | A/G | 1.82693e-05 | 0.00302231 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996850 | GAGCGGGAGCGGGTA[A/G]AAGGGGCTCTAGGCC | 79058 |
| rs760994007 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016886 | TAAGTGCCGGTGGGT[A/C]TGGGGGCACCTCCCG | 79058 |
| rs760994589 | snp | C/T | 2.70215e-05 | 0.0036756 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012126 | TGAGGGGCTCTTCTG[C/T]CCCACTTGAGGCGTC | 79058 |
| rs761014187 | in-del | -/TCTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982745 | TTCTTTCTTGTTTTC[-/TCTT]TCTTTCTTTCTTTCT | 79058 |
| rs761018784 | snp | A/G | 2.75904e-05 | 0.00371409 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983693 | GCTCTGGGGGAGGCT[A/G]ACTGTGTGGGGCACA | 79058 |
| rs761122088 | snp | C/T | 3.32265e-05 | 0.0040758 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985500 | TCTCATGTCTTATAC[C/T]CTCCAGGTTCGCATC | 79058 |
| rs761183748 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005502 | TGAGTGAGACTGACC[C/G]CAGCAGCTTCCTGAG | 79058 |
| rs761345535 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976381 | AGGTTGCACAGAGCA[C/T]GGGACTGGCTGGCTG | 79058 |
| rs761368957 | snp | C/T | 0.000155994 | 0.00883021 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009046 | CTCCAGCCCGTGGAC[C/T]GGGAGCCCGTGGACC | 79058 |
| rs761379437 | snp | A/C/G | 3.36526e-05 | 0.00410188 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016961 | TGTCCAGGGCCGCCG[A/C/G]GTCCCCTTCCCCATT | 79058 |
| rs761437153 | snp | C/T | 0.000116122 | 0.00761889 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985572 | CTGTTCAGGCCAGAC[C/T]CTCTGGGAGCTTCTC | 79058 |
| rs761473166 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980493 | CAGGTGGTCTTGGGC[C/T]TTCTGCCCCAGACCT | 79058 |
| rs761488078 | snp | A/G | 3.4421e-05 | 0.00414841 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996563 | TGAGCCGTCCGGAGG[A/G]CGCGGACACCTCAGG | 79058 |
| rs761508654 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985762 | GAGGAGGGGTGTGTG[A/G]GCTGCCGGTTCATGA | 79058 |
| rs761580508 | snp | G/T | 1.78851e-05 | 0.00299036 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015244 | CCTCTCCAAGCACTG[G/T]TCAGCCTCCATGCCA | 79058 |
| rs761633539 | snp | G/T | 1.73324e-05 | 0.00294379 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017378 | CCACCTCCTCTGCCA[G/T]CAGGAATAAAGACTT | 79058 |
| rs761675460 | snp | C/T | 0.000317763 | 0.0126008 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977762 | AGGTGCGGCCGCCCG[C/T]CCGGGGCGGACGGGT | 79058 |
| rs761709939 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989692 | GCCACGTGTTTGAAA[C/T]GTTGCAGCTCCACTG | 79058 |
| rs761729576 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002848 | CAGGCGTGAGCCACC[A/G]CGCCCGGCCTGTTTT | 79058 |
| rs761748454 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984147 | AGGCGTGAGCCTCTG[C/T]GCCCCGCCCACGTCA | 79058 |
| rs761793658 | snp | C/T | 1.78953e-05 | 0.00299121 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015179 | GGTAGGAGATGGAGG[C/T]GACGTGGACTCTGGG | 79058 |
| rs761808054 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989897 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCACCT | 79058 |
| rs761817126 | snp | A/G | 5.04995e-05 | 0.00502466 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017332 | AGGTGAGAGCTGCCA[A/G]CCTGAGGTGCCCACT | 79058 |
| rs761826398 | in-del | -/AGCCCGTGGACCGGG | 0.00842714 | 0.0643627 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:82009034 | GCGCCCTCTGCCTCC[-/AGCCCGTGGACCGGG]AGCCCGTGGACCGGG | 79058 |
| rs761840023 | snp | A/G | 3.60848e-05 | 0.00424748 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996839 | AGCAGGAGCAGGAGC[A/G]GGAGCGGGTAAAAGG | 79058 |
| rs761871880 | snp | C/T | 0.00012181 | 0.00780322 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995001 | GGGCTCTTGAAAGCA[C/T]GACGTGTTTCATGGA | 79058 |
| rs761893252 | snp | A/G | 1.65963e-05 | 0.0028806 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011588 | ACCTGGGGAACCCCG[A/G]GCTGTCATTTTACCT | 79058 |
| rs761954141 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982792 | TTTTTCTTCCTTTCT[C/T]TTTTCTTTTCTTTTC | 79058 |
| rs761999204 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013520 | AGAGCTGGCGGGGCT[A/G]AGGGAAGGAAGCCTG | 79058 |
| rs762029802 | snp | A/G | 3.5895e-05 | 0.0042363 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015299 | ACCATCCCCTCGTCC[A/G]AGCAGTGGCGATCCC | 79058 |
| rs762100613 | snp | A/C/T | 0.000100196 | 0.00707742 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011532 | CTGTATGTTCTTTTT[A/C/T]TCCTCTGCAGTGGGG | 79058 |
| rs762130859 | snp | C/G | 1.97916e-05 | 0.0031457 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016786 | GCTCAGGGTGAGCTT[C/G]GGCCTCCCTGCAGGT | 79058 |
| rs762184697 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995452 | CCAGCACTGTCCTGA[A/G]GCTGTGGCCCTCAGG | 79058 |
| rs762187602 | snp | A/G | 2.20841e-05 | 0.00332288 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996070 | GCCACCATCAGGTAA[A/G]GGCAGTGCTGCTGGG | 79058 |
| rs762209999 | in-del | -/CTCCTTCCTCCGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013225 | GGGCGGACTCCGGGC[-/CTCCTTCCTCCGT]CTCCATCCCCTCCCT | 79058 |
| rs762224849 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003249 | CTAGGGGTTTTAGAC[C/G]AGCCTGGGCAACATA | 79058 |
| rs762233864 | snp | G/T | 2.54185e-05 | 0.00356491 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983683 | GGTGGGTCGTGCTCT[G/T]GGGGAGGCTGACTGT | 79058 |
| rs762239951 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014335 | TACCCCACCTGGACC[C/G]TCTGAAATGTTCCTC | 79058 |
| rs762261393 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992433 | TGGCGTTTGATGTCA[C/T]GCTGCTGTGCTCTGT | 79058 |
| rs762270992 | snp | C/T | 0.000190749 | 0.00976412 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009521 | CCTTGGTGACCAAGG[C/T]CTTCAGGGAGGCGCA | 79058 |
| rs762291072 | snp | A/C/T | 3.70928e-05 | 0.00430643 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996396 | CACCACAAGGTGCTT[A/C/T]CCTTGTCCTCTGGCC | 79058 |
| rs762319828 | snp | C/T | 5.6224e-05 | 0.00530178 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015064 | CGGTGTGACCCACTT[C/T]CCCTTTCCAGCCCCA | 79058 |
| rs762322339 | snp | A/G | 3.0633e-05 | 0.00391351 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009225 | CCTCCCGGCATCTTC[A/G]CGCCAGGGTTTGCCC | 79058 |
| rs762407992 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986841 | CGCTGCATGGCACGG[A/G]TGTTGCGTTCGTGGG | 79058 |
| rs762509922 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998806 | GGTTCTGGAAGTTCT[C/G]CGAAGGTTATGGCCA | 79058 |
| rs762523091 | snp | A/T | 3.3335e-05 | 0.00408245 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009538 | TTCAGGGAGGCGCAG[A/T]TAAAGGAGAAGCTGG | 79058 |
| rs762569501 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987691 | CTTAGTTTAAGAAAC[A/G]ACAGGCTTGGCCAGG | 79058 |
| rs762611965 | snp | G/T | 1.64768e-05 | 0.00287021 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979200 | TTCTGGAGGACACGT[G/T]CCGGCGGCAGGACTT | 79058 |
| rs762620712 | snp | A/G | 0.000715563 | 0.0189016 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977732 | TGAAGGTGACGCCGA[A/G]CACCGTGCTGCTTCA | 79058 |
| rs762671756 | in-del | -/TT | 0.0600282 | 0.162514 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010088 | GGCTAATTTTTGTTG[-/TT]TTTTTTTTTTTTACT | 79058 |
| rs762710804 | snp | C/T | 5.3711e-05 | 0.00518195 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015159 | CAGAGAACACGCTTG[C/T]CAGTGGTAGGAGATG | 79058 |
| rs762736907 | snp | A/G | | | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011604 | GCTGTCATTTTACCT[A/G]TGTACGTTTTTTCTC | 79058 |
| rs762786733 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980541 | AGTCTCTCTTGTCAA[A/C]TGAAGAATGCGGTTC | 79058 |
| rs762807757 | snp | C/T | 1.76253e-05 | 0.00296856 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996821 | AGCGGGAGCGGGATC[C/T]CCAGCAGGAGCAGGA | 79058 |
| rs762873899 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991526 | CATGCTGCTGGGCCA[C/G]CTCAGAGCTCTGCGG | 79058 |
| rs762947337 | in-del | -/TG | 3.35278e-05 | 0.00409424 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016920 | CGGCACTCACCACTC[-/TG]TGTCTTCGCCTCCCC | 79058 |
| rs762966859 | snp | A/G | 2.42969e-05 | 0.00348538 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017154 | GTGCTGTGGCCGGGT[A/G]GAGGGCGGGGGTCCG | 79058 |
| rs762974117 | snp | A/G | | | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009098 | CCGACCTGGAGGAGC[A/G]GCTGCAGGCCTGGCC | 79058 |
| rs763006339 | snp | C/T | 3.3195e-05 | 0.00407387 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011584 | AGCCACCTGGGGAAC[C/T]CCGAGCTGTCATTTT | 79058 |
| rs763059544 | snp | A/C/T | 3.34109e-05 | 0.00408712 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011530 | GTCTGTATGTTCTTT[A/C/T]TCTCCTCTGCAGTGG | 79058 |
| rs763116176 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003106 | GCCGGCCTTGGCCTC[C/T]GAAAGAGCTGGCATT | 79058 |
| rs763150323 | snp | G/T | 2.28225e-05 | 0.00337797 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983672 | CCTGAGAACATGGTG[G/T]GTCGTGCTCTGGGGG | 79058 |
| rs763193320 | snp | C/T | 0.000116344 | 0.00762616 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985497 | GTTTCTCATGTCTTA[C/T]ACCCTCCAGGTTCGC | 79058 |
| rs763244054 | snp | C/G | 8.14697e-05 | 0.00638187 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015364 | CAGGCCGGGTAGGCT[C/G]CCTGGCTCAGTGCTC | 79058 |
| rs763359774 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995770 | AGGCTGGGGGAGACA[C/G]GGTCAGGCATGGGCA | 79058 |
| rs763382388 | snp | C/T | 1.66402e-05 | 0.00288441 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012204 | GTCCACGGTGCTTCC[C/T]AACACGTAGGTGCCT | 79058 |
| rs763399163 | snp | A/G | 2.1571e-05 | 0.00328406 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996053 | GCCTGACCGGGGGCA[A/G]CGCCACCATCAGGTA | 79058 |
| rs763422905 | snp | C/T | 2.84953e-05 | 0.0037745 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009218 | CTCAGTGCCTCCCGG[C/T]ATCTTCGCGCCAGGG | 79058 |
| rs763450436 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014720 | TGGGCCACGTGTGCA[G/T]GCAGCCCCTACAGAG | 79058 |
| rs763462296 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007628 | AGGGGTACTCTGCCC[A/G]CCTGGGAAGACAGTG | 79058 |
| rs763469489 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993716 | CTGACCCTCCCAGTA[C/G]CCCCCATCCCGGAGG | 79058 |
| rs763494271 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984718 | CTTTTGAAGCCCCCA[C/G]TGGGACACGAGGACT | 79058 |
| rs763529502 | snp | A/T | 3.4167e-05 | 0.00413308 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016827 | AGCCTGGCCTGCTGG[A/T]GCATGCCATCTCCCC | 79058 |
| rs763537894 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975943 | GAAAGTGACTATAAA[G/T]GTAGAAGAAACAATA | 79058 |
| rs763588776 | in-del | -/A | 1.77855e-05 | 0.00298202 | utr-variant-3-prime, nc-transcript-variant, frameshift-variant | ASPSCR1 | GRCh38.p7 | 17:82017386 | TCTGCCAGCAGGAAT[-/A]AAGACTTGTGCATCC | 79058 |
| rs763608928 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994034 | TTTCACGGTGGGGAG[C/T]TGGAAACGCAGAGGC | 79058 |
| rs763657202 | snp | C/G | 1.66549e-05 | 0.00288568 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994814 | GGTTTCTTTCCTCTC[C/G]TCCCAGGGAGTGCCT | 79058 |
| rs763785389 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985160 | TGCACGCACATGCGC[A/G]CACCTGCACACACCC | 79058 |
| rs763822190 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008413 | GAGTGTGGGTCGGCG[-/C]AGTGCTGAGGTGTCC | 79058 |
| rs763824695 | snp | A/G | 1.77792e-05 | 0.00298149 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996437 | TTGTCATGAAGTGCT[A/G]CGACCCCGTGGGCAA | 79058 |
| rs763879641 | snp | A/G | 0.000123365 | 0.00785286 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009540 | CAGGGAGGCGCAGAT[A/G]AAGGAGAAGCTGGAG | 79058 |
| rs763916810 | snp | A/G | 8.94895e-05 | 0.00668855 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015172 | TGCCAGTGGTAGGAG[A/G]TGGAGGCGACGTGGA | 79058 |
| rs763937377 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001308 | CTGACGCCGGGCTAG[A/G]CAGGAGCCCCCACAT | 79058 |
| rs763953681 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988771 | GTCATGTGGGTGTTG[C/T]GGGGCATCTGGCTGT | 79058 |
| rs763960309 | in-del | -/G | 5.06624e-05 | 0.00503276 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983682 | GGTGGGTCGTGCTCT[-/G]GGGGGAGGCTGACTG | 79058 |
| rs764048749 | snp | A/G | | | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996833 | ATCCCCAGCAGGAGC[A/G]GGAGCGGGAGCGGGT | 79058 |
| rs764061434 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006723 | GCCCTGCAGGGCCCT[C/T]GCTGTCGCTTTTTTC | 79058 |
| rs764091388 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990179 | CCCAAAATACGACTT[C/T]CTGGACACGTAGTCA | 79058 |
| rs764101723 | snp | A/G | 1.69049e-05 | 0.00290726 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996746 | TCTCCAGCCCTGGAG[A/G]CCCCTCCAAGCCAAA | 79058 |
| rs764117039 | snp | A/G | 3.94555e-05 | 0.00444142 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015091 | CCCAGCTTGGTGACC[A/G]GGTGGCTCCATTCAC | 79058 |
| rs764166839 | in-del | -/AGCAGG | 0.000282888 | 0.0118897 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996823 | GGGAGCGGGATCCCC[-/AGCAGG]AGCAGGAGCAGGAGC | 79058 |
| rs764170532 | snp | C/T | 4.97475e-05 | 0.00498711 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017160 | TGGCCGGGTGGAGGG[C/T]GGGGGTCCGGGTGCT | 79058 |
| rs764194199 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982260 | AGGCATGAGCCACCG[C/T]GCCCAGCGCATTGTT | 79058 |
| rs764223425 | snp | C/G | 1.93744e-05 | 0.00311237 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017084 | TGAAGAGGAGCCTGG[C/G]CAAGGTGCCCAAGTG | 79058 |
| rs764296507 | snp | A/G | 1.68545e-05 | 0.00290292 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996658 | CCTTTCTCGGGTGGG[A/G]GACAGAGACTGGGGG | 79058 |
| rs764310473 | snp | C/T | 2.17068e-05 | 0.00329438 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996054 | CCTGACCGGGGGCAG[C/T]GCCACCATCAGGTAA | 79058 |
| rs764353804 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982679 | TTGCATTTCCAAAGT[A/G]AGGCCAACCACTTTG | 79058 |
| rs764355939 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993184 | GTTCTCATTTCAGGG[A/G]GGCAAGTCCTGCCCT | 79058 |
| rs764386900 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000308 | TCGCCCGTCGGGAGG[C/T]GCTGTTGGGGTGGGG | 79058 |
| rs764426390 | snp | C/T | 2.0708e-05 | 0.0032177 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016489 | AGGCGAACCTCTTCC[C/T]GGCCGCTCTGGTGCA | 79058 |
| rs764446354 | snp | A/G | 1.78497e-05 | 0.00298739 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983626 | CAATGCCAAGCTGGA[A/G]ATGGTGCCCGCTTCC | 79058 |
| rs764467045 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004780 | CAAGAGGGGCAGGGT[C/G]GGGAAGAAGGGAGTG | 79058 |
| rs764504665 | snp | C/T | 5.71608e-05 | 0.00534576 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009220 | CAGTGCCTCCCGGCA[C/T]CTTCGCGCCAGGGTT | 79058 |
| rs764607835 | snp | G/T | 2.26626e-05 | 0.00336613 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:81983553 | CTGGTCTGTCTTGCA[G/T]GTTTCAGAGGAGCGT | 79058 |
| rs764612560 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010560 | AAAAAAAACCAGCAC[A/G]TTTGAACCCAGGTCA | 79058 |
| rs764627406 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011108 | AGCCCGTGGTCCTGA[A/G]TGCTCACGTCGCCCA | 79058 |
| rs764666679 | snp | A/T | 1.82251e-05 | 0.00301864 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996414 | TTGTCCTCTGGCCCC[A/T]CTCAGGTTTGTCATG | 79058 |
| rs764725002 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978693 | TGCCAGGCGTGCAGA[A/G]TGCGGAAGTGGGGCG | 79058 |
| rs764733907 | snp | C/T | 3.81148e-05 | 0.00436531 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017439 | TCCTCCAGAAAAGGG[C/T]CCCCGTCGTCTGCCC | 79058 |
| rs764851525 | snp | C/T | 2.13345e-05 | 0.003266 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015081 | CCTTTCCAGCCCCAG[C/T]TTGGTGACCGGGTGG | 79058 |
| rs764861573 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985826 | TCGTTCTGAGTTTCC[A/T]GGGCCCAGCGGCCCA | 79058 |
| rs764882862 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986688 | GCTGGTGTGTGGATG[G/T]GGTGAGTTCATGTCT | 79058 |
| rs764892951 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001592 | GAACCCCGGGGGGTA[-/G]GGGGTGGATGCTCGC | 79058 |
| rs764940254 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002322 | GGAGTACAATGGCAC[A/G]ATCTCGGCTCACTGC | 79058 |
| rs764951155 | snp | C/T | 5.02744e-05 | 0.00501345 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016905 | GGGCACCTCCCGTGG[C/T]GGCACTCACCACTCT | 79058 |
| rs764993519 | snp | A/G | 1.66402e-05 | 0.00288441 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009242 | GCCAGGGTTTGCCCC[A/G]TCGGGTGCTTGTGCT | 79058 |
| rs765038456 | snp | C/T | 1.66969e-05 | 0.00288932 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012323 | CTGCGGGGCGGGGCC[C/T]TCCAGGGAGGGCAGG | 79058 |
| rs765054267 | snp | A/G | 1.66582e-05 | 0.00288597 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994830 | TCCCAGGGAGTGCCT[A/G]CAGCACCCCGGCGGG | 79058 |
| rs765090336 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990705 | GATTTCATGGCCTAC[A/G]GGCCCTGGGGGTACA | 79058 |
| rs765090394 | snp | A/G | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979106 | ACCAGGAAGCTGAAT[A/G]CCCTTGGCTGACCTG | 79058 |
| rs765133691 | snp | A/G | | | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994872 | CTGCGTGTACACGAG[A/G]GATGAGGTAGGCGGC | 79058 |
| rs765135115 | snp | A/G | 1.89396e-05 | 0.00307724 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017075 | CCCAGCCCGTGAAGA[A/G]GAGCCTGGGCAAGGT | 79058 |
| rs765136927 | snp | C/T | 1.74931e-05 | 0.0029574 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994907 | TCTTGCTCACCCAGT[C/T]CCCGCTCACTTTCAG | 79058 |
| rs765187547 | snp | C/T | 3.36304e-05 | 0.0041005 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996728 | CTAAGTTGCCGAAGT[C/T]CCTCTCCAGCCCTGG | 79058 |
| rs765223519 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008019 | CTCCCGCCAGACTCC[C/T]GTGACAAGTCATAAC | 79058 |
| rs765295747 | snp | C/G | 3.52417e-05 | 0.00419757 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983603 | TGGAGATTTGCCAAC[C/G]TGCCCAACAATGCCA | 79058 |
| rs765374414 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006818 | GCGCGGGAGCGGCGC[A/T]GATGCCACAAATGCG | 79058 |
| rs765467443 | snp | C/T | 2.62822e-05 | 0.00362497 | downstream-variant-500B, intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017425 | CTTCCTGTCATGCTT[C/T]CTCCAGAAAAGGGCC | 79058 |
| rs765479614 | snp | C/T | 1.79187e-05 | 0.00299317 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015288 | CCCTCCTCTCCACCA[C/T]CCCCTCGTCCGAGCA | 79058 |
| rs765492765 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995672 | TCGCTCCGGGCAGTG[A/G]GTCCTGGCACCAGGG | 79058 |
| rs765505616 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005297 | GGCATCAGTTGGGCC[C/T]TGGGGTTTGGTCTCG | 79058 |
| rs765583398 | snp | C/T | 6.65875e-05 | 0.00576969 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996009 | GACGGGTGAAGCTGC[C/T]CTGCGGGGCACGACG | 79058 |
| rs765590616 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992549 | GGCCTCCCCAGCCGT[A/G]GAGAAGTGGCCTCAT | 79058 |
| rs765628303 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013564 | CAAGCAGGCGGCGGG[C/T]GCGGAAGCACCAGCT | 79058 |
| rs765651899 | snp | A/C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006428 | AAAGTGAATGCAGCC[A/C/G]AATGATCACATCTGC | 79058 |
| rs765812603 | snp | C/T | 0.00018648 | 0.00965429 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009226 | CTCCCGGCATCTTCG[C/T]GCCAGGGTTTGCCCC | 79058 |
| rs765819740 | snp | G/T | 0.000125431 | 0.00791832 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012137 | TCTGCCCCACTTGAG[G/T]CGTCACCCCCATCTG | 79058 |
| rs765831523 | snp | C/G | 1.71164e-05 | 0.00292539 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009053 | CCGTGGACCGGGAGC[C/G]CGTGGACCGGGAGCC | 79058 |
| rs765836368 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982278 | CCAGCGCATTGTTAC[C/T]TCTCAGTGTTCACCT | 79058 |
| rs765843326 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986845 | GCATGGCACGGGTGT[C/T]GCGTTCGTGGGTGAG | 79058 |
| rs765948126 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976362 | GTGGCTCAGTAAGGT[A/T]CTGAGGTTGCACAGA | 79058 |
| rs765973338 | in-del | -/AGG | 6.17036e-05 | 0.0055541 | cds-indel, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009542 | GGGAGGCGCAGATAA[-/AGG]AGAAGCTGGAGCGCT | 79058 |
| rs766001170 | snp | C/T | 8.34341e-05 | 0.00645834 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012316 | TGGGGTGCTGCGGGG[C/T]GGGGCCCTCCAGGGA | 79058 |
| rs766003319 | snp | A/G/T | 6.68342e-05 | 0.00578043 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009167 | ACGACGTGAGAAGAC[A/G/T]CTTGGCCCAGCTCAA | 79058 |
| rs766077391 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992740 | TGAGCCCTGCGTCTC[A/G]GGGCCTCTGGGCCGA | 79058 |
| rs766085209 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982073 | TCCCGGGTTGAAGCA[C/T]TCCTCCCACTTCAGC | 79058 |
| rs766119047 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980746 | AATACGCTGTAGGAG[A/G]ATCATGAGTATTCAT | 79058 |
| rs766133828 | in-del | -/T | 0.222149 | 0.248444 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010088 | GGCTAATTTTTGTTG[-/T]TTTTTTTTTTTTTAC | 79058 |
| rs766143738 | snp | C/G | 1.69315e-05 | 0.00290955 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996636 | ACCCGCAGCTGCCCC[C/G]TTTGTTCCTTTCTCG | 79058 |
| rs766180144 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002850 | GGCGTGAGCCACCGC[A/G]CCCGGCCTGTTTTCA | 79058 |
| rs766219452 | snp | G/T | 1.66466e-05 | 0.00288496 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985602 | CAGCCATTTTCCACA[G/T]ATCAGGTGAGCATCA | 79058 |
| rs766231368 | snp | C/T | 3.35813e-05 | 0.0040975 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983506 | GCGTGGATGGCAGGG[C/T]GTGTCAGGCTCTGCA | 79058 |
| rs766253192 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985858 | CCTTGCCCACCTAGA[A/G]GAGCAGGAATGTGCT | 79058 |
| rs766327377 | snp | C/T | 3.57929e-05 | 0.00423027 | stop-gained, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015270 | TGCCACCCAGTCTGC[C/T]GACCCTCCTCTCCAC | 79058 |
| rs766340477 | snp | A/G | 3.35419e-05 | 0.00409509 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010873 | CAGCGAGACAGGTGG[A/G]CAGCGCTGTGGGGTG | 79058 |
| rs766398613 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003118 | CTCCGAAAGAGCTGG[A/C]ATTACAGGCGTGAGC | 79058 |
| rs766406184 | snp | C/T | 4.98716e-05 | 0.00499333 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011609 | CATTTTACCTGTGTA[C/T]GTTTTTTCTCCTGAG | 79058 |
| rs766418016 | snp | C/T | 1.71811e-05 | 0.00293091 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996575 | AGGACGCGGACACCT[C/T]AGGGCCCTGCTGCGA | 79058 |
| rs766457198 | in-del | -/AAAAG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987864 | AAAAAACAAAAAAAC[-/AAAAG]AAACAACAAGGCTGG | 79058 |
| rs766457466 | snp | A/C | 0.000113339 | 0.00752706 | downstream-variant-500B, intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017413 | ATCCCTCAACGCCTT[A/C]CTGTCATGCTTCCTC | 79058 |
| rs766491810 | snp | C/T | 5.36764e-05 | 0.00518028 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015191 | AGGCGACGTGGACTC[C/T]GGGAGGCTTCTTTTT | 79058 |
| rs766497380 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991613 | CCTGTCCATCCCTGT[C/G]CATCCTTGTCCATCC | 79058 |
| rs766517942 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007192 | TCGGGGCTGCTCTGC[C/G]CAGGTGAAGGGCGGG | 79058 |
| rs766534205 | snp | C/T | 0.000163239 | 0.00903287 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995010 | AAAGCACGACGTGTT[C/T]CATGGAAAAAGAGGG | 79058 |
| rs766537048 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979222 | GCAGGACTTCAACCC[C/T]TGTGAATATGATCTG | 79058 |
| rs766563404 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979925 | ATGGATAGGATGTGC[A/G]TGTCTATCCCACACG | 79058 |
| rs766594216 | snp | C/G | 2.8099e-05 | 0.00374816 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995946 | GCTTCCCTGGGCTCT[C/G]GGGTCCCGGTGCAAG | 79058 |
| rs766599436 | in-del | -/TCTTTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982769 | CTTTCTTTCTTCTTC[-/TCTTTT]TCTTTTTCTTCCTTT | 79058 |
| rs766654217 | snp | C/T | 1.70151e-05 | 0.00291672 | utr-variant-3-prime, nc-transcript-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017344 | CCAGCCTGAGGTGCC[C/T]ACTCCGCCAGCCACA | 79058 |
| rs766689980 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990835 | AGTTTCTCTCCATGG[A/G]TTTAGAGCCAGCAGG | 79058 |
| rs766708030 | in-del | -/AGTC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010382 | AAAATACAAAAAATT[-/AGTC]AGGAGAGGTGGCGCA | 79058 |
| rs766733579 | snp | A/G | 0.000182665 | 0.00955506 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009040 | CTCTGCCTCCAGCCC[A/G]TGGACCGGGAGCCCG | 79058 |
| rs766786537 | snp | C/T | 1.87883e-05 | 0.00306493 | intron-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996872 | CTCTAGGCCTTGGGA[C/T]TTGGGGGTGTCCTTT | 79058 |
| rs766809331 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994696 | CCTGGGCCTGGGACG[C/G]TGTCCTGGGTGGGTG | 79058 |
| rs766818432 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983033 | ATTTTCAGTAGAGAC[A/G]GGGTTTCACCATGTT | 79058 |
| rs766844361 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015429 | CCCAGGCCTGGCTGC[C/T]AAGCCTACTTCCCTC | 79058 |
| rs766899647 | snp | A/G | 1.73854e-05 | 0.00294829 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996487 | TCGTCAGCGTCGGCT[A/G]GCCAGGCAGCCGCCA | 79058 |
| rs766930175 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014735 | TGCAGCCCCTACAGA[A/G]TTGCTGCCCCGTGGG | 79058 |
| rs766947578 | snp | C/T | 8.9021e-05 | 0.00667103 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016808 | CCTGCAGGTGTCTAC[C/T]TGGAGCCTGGCCTGC | 79058 |
| rs767050329 | snp | C/T | 1.66073e-05 | 0.00288156 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985587 | CCTCTGGGAGCTTCT[C/T]AGCCATTTTCCACAG | 79058 |
| rs767051596 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984725 | AGCCCCCACTGGGAC[A/T]CGAGGACTGTCTCCA | 79058 |
| rs767061864 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995823 | ACCAGACTCAAGCTG[A/G]GCCTTGTGGAGGGTG | 79058 |
| rs767063165 | in-del | -/G | 0.000815328 | 0.0201742 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010090 | TAATTTTTGTTGTTT[-/G]TTTTTTTTTTTACTA | 79058 |
| rs767104735 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81998165 | TCATAAAGACGAGGT[C/T]TCTCTCTGTTGCCCA | 79058 |
| rs767117214 | snp | C/T | 1.6661e-05 | 0.00288621 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994808 | CCTGATGGTTTCTTT[C/T]CTCTCCTCCCAGGGA | 79058 |
| rs767142775 | snp | A/C/G | 2.45378e-05 | 0.00350261 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012139 | TGCCCCACTTGAGGC[A/C/G]TCACCCCCATCTGCA | 79058 |
| rs767189813 | in-del | -/AAG | 1.95109e-05 | 0.00312331 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017086 | AAGAGGAGCCTGGGC[-/AAG]GTGCCCAAGTGGCTG | 79058 |
| rs767199991 | snp | C/T | 1.67635e-05 | 0.00289507 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016925 | CTCACCACTCTGTGT[C/T]TTCGCCTCCCCACAG | 79058 |
| rs767225415 | snp | A/G | 1.65875e-05 | 0.00287984 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985513 | ACCCTCCAGGTTCGC[A/G]TCGCTTTGCAGCTGG | 79058 |
| rs767231230 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996267 | GTCCCCCAGAGGGGC[A/G]GTGGATCTTGGGAGG | 79058 |
| rs767256007 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993789 | ATCCCCTGTGTTCTG[A/G]TCACCAGCTCAGCCT | 79058 |
| rs767421088 | snp | A/G | 1.64762e-05 | 0.00287016 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979204 | GGAGGACACGTGCCG[A/G]CGGCAGGACTTCAAC | 79058 |
| rs767422195 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987013 | TCAGACAACAGTGAC[A/G]GAGCCTAAGAGCAAA | 79058 |
| rs767474087 | snp | C/T | 2.8047e-05 | 0.00374469 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995942 | GAGGGCTTCCCTGGG[C/T]TCTGGGGTCCCGGTG | 79058 |
| rs767476847 | snp | C/T | 0.000107315 | 0.00732435 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015252 | AGCACTGGTCAGCCT[C/T]CATGCCACCCAGTCT | 79058 |
| rs767477848 | snp | G/T | 0.000381025 | 0.0137974 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977767 | CGGCCGCCCGCCCGG[G/T]GCGGACGGGTAGGCG | 79058 |
| rs767495223 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000237 | GGCGGGTCTTGTCTG[A/C]AGAGCGTGGGGCGTG | 79058 |
| rs767531415 | snp | A/G | 1.74069e-05 | 0.00295011 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995002 | GGCTCTTGAAAGCAC[A/G]ACGTGTTTCATGGAA | 79058 |
| rs767595442 | snp | A/G | 3.6735e-05 | 0.00428557 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015112 | CTCCATTCACCCTGG[A/G]TCCCTCGCTGAAACG | 79058 |
| rs767650904 | snp | A/G | 2.37071e-05 | 0.00344282 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017165 | GGGTGGAGGGCGGGG[A/G]TCCGGGTGCTGTGGC | 79058 |
| rs767688268 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81988399 | GGCGGAGGTTGTAGT[C/G]AGCTGAGATTGCGCC | 79058 |
| rs767775739 | snp | C/T | 0.000108929 | 0.00737919 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996844 | GAGCAGGAGCGGGAG[C/T]GGGTAAAAGGGGCTC | 79058 |
| rs767815661 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011876 | GCACCCCAGCCTGGT[C/T]CCCACCCCTGGGGCT | 79058 |
| rs767828835 | snp | A/G | 2.5549e-05 | 0.00357405 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983685 | TGGGTCGTGCTCTGG[A/G]GGAGGCTGACTGTGT | 79058 |
| rs767839387 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981310 | TTCAAGGTTTCTGGG[A/G]TCCCCTGGGCCAAGA | 79058 |
| rs767951354 | snp | C/T | 1.94105e-05 | 0.00311526 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016789 | CAGGGTGAGCTTGGG[C/T]CTCCCTGCAGGTGTC | 79058 |
| rs767989654 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004444 | GGGGGCCTGGGTTTG[C/T]AGGAGACAGGAAGGG | 79058 |
| rs768077501 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003386 | CTGAGAGATCAAGAC[C/T]GCAGTGAGCTGAGAT | 79058 |
| rs768079151 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979759 | GCTGGCCGTGGAGAA[A/C]TAGGATGCCTTGAAA | 79058 |
| rs768096684 | snp | A/G | 0.000136902 | 0.00827238 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996080 | GGTAAGGGCAGTGCT[A/G]CTGGGGCCGAGGAGT | 79058 |
| rs768224952 | snp | A/G/T | 6.67784e-05 | 0.00577801 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010854 | TACAGGGCTTCTTCC[A/G/T]CCCCAGCGAGACAGG | 79058 |
| rs768281745 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011032 | GGTGCAGAGGCATCC[C/T]AGTTCGCAGAGTGTC | 79058 |
| rs768298348 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008814 | CTGACTGGGAGAGGG[C/G]GGTCTCCAGCCCTGG | 79058 |
| rs768306343 | snp | C/G | 2.62299e-05 | 0.00362136 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995968 | CGGTGCAAGGCGCAC[C/G]TGTCCTGGCTGCTCC | 79058 |
| rs768309316 | snp | A/G | 3.29707e-05 | 0.00406008 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979277 | GCAGGGTCTGAGTAT[A/G]TCTGTGCCCCTGCCC | 79058 |
| rs768325346 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991192 | AGCCATGGAGGGGAT[A/T]TGTCCTCTCTCAGAG | 79058 |
| rs768355936 | snp | C/T | 0.000342424 | 0.0130803 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017149 | GTGGGGTGCTGTGGC[C/T]GGGTGGAGGGCGGGG | 79058 |
| rs768392610 | snp | A/G | 3.3269e-05 | 0.00407841 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010812 | CCTAGGTGGCTCTGA[A/G]GGTCCTGTTCCCCGA | 79058 |
| rs768399489 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980380 | CTTACGAGGCTCTCC[G/T]GGGAGGAGTTTCTTA | 79058 |
| rs768446085 | snp | C/T | 3.57711e-05 | 0.00422898 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015241 | GAGCCTCTCCAAGCA[C/T]TGGTCAGCCTCCATG | 79058 |
| rs768500602 | snp | C/T | 0.00250941 | 0.0353328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995071 | CGAAACCTCCCTCGG[C/T]GCCCTGTTTGTTTTT | 79058 |
| rs768552187 | snp | C/T | 0.00056164 | 0.0167483 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009009 | CCAGCCCGTGACACC[C/T]GCCGTCAGCCGCGCC | 79058 |
| rs768655411 | in-del | -/CCGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000296 | CCCGCCCGTGCTCGC[-/CCGT]CCGTCGGGAGGCGCT | 79058 |
| rs768660102 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010389 | AAAAAATTAGTCAGG[A/C]GAGGTGGCGCACGCC | 79058 |
| rs768673621 | in-del | -/T/TT | 0.00659095 | 0.0570902 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010084 | CTCGGCTAATTTTTG[-/T/TT]TTGTTTTTTTTTTTT | 79058 |
| rs768702841 | snp | A/T | 1.68306e-05 | 0.00290087 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017327 | GCAAGAGGTGAGAGC[A/T]GCCAGCCTGAGGTGC | 79058 |
| rs768704797 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003854 | CCTCCGAGGGTGGCC[A/G]GGGCGCTGAGTAACT | 79058 |
| rs768714245 | snp | A/G | 1.67175e-05 | 0.0028911 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016868 | GATGTGCTGGTGGCC[A/G]GGTAAGTGCCGGTGG | 79058 |
| rs768725272 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002506 | GTGATCCACTTGCAT[C/T]GGCCTCCCAAAGTGC | 79058 |
| rs768743187 | snp | C/T | 0.000756794 | 0.0194377 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996473 | CAGGAAGCCTGGGCT[C/T]GTCAGCGTCGGCTGG | 79058 |
| rs768776239 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994366 | GAAGGAGGACATCAG[A/G]CGGTGGAGACAGGGG | 79058 |
| rs768964601 | in-del | -/CC | 1.66272e-05 | 0.00288328 | intron-variant, frameshift-variant | ASPSCR1 | GRCh38.p7 | 17:82012211 | TGCTTCCTAACACGT[-/CC]AGGTGCCTTCTCTCC | 79058 |
| rs768976092 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014242 | CACCCAGGACAGCCC[C/T]GTCCTGCACTGCCGT | 79058 |
| rs768981143 | snp | C/T | 4.69351e-05 | 0.00484411 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983675 | GAGAACATGGTGGGT[C/T]GTGCTCTGGGGGAGG | 79058 |
| rs769008728 | snp | A/C | 7.11516e-05 | 0.00596412 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009500 | GGAAGCGCCTGGAAG[A/C]AGCCCCCTTGGTGAC | 79058 |
| rs769033757 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981166 | GAGAGAAGGGCCTGG[A/C]GGGAGGTTGGCTGAT | 79058 |
| rs769048147 | snp | C/T | 1.6777e-05 | 0.00289624 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994868 | CAGTCTGCGTGTACA[C/T]GAGGGATGAGGTAGG | 79058 |
| rs769088800 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004332 | TCTGGCCTTTCTCCG[A/G]CCCCCTTCCAGTTTC | 79058 |
| rs769106453 | snp | A/G | 0.000571265 | 0.016891 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977658 | GAAAATGGCGGCCCC[A/G]GCAGGCGGCGGAGGC | 79058 |
| rs769145214 | snp | A/G | 3.52193e-05 | 0.00419624 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015051 | CTGGCTGGGGGGACG[A/G]TGTGACCCACTTTCC | 79058 |
| rs769159590 | snp | C/T | 2.29182e-05 | 0.00338505 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994959 | CTGCTGTCCCGCAGC[C/T]GTCTCCAGGGCAGTG | 79058 |
| rs769188171 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006389 | TGCACATATGTGCAT[A/G]CATGTTTGCCCCAGA | 79058 |
| rs769200156 | snp | A/C | 1.66427e-05 | 0.00288462 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012296 | CAGGTACCTGAGGGC[A/C]TCCCTGGGGTGCTGC | 79058 |
| rs769244382 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979788 | AAACTGCAGGTGGAT[-/C]CCTGCAGTCTCACAG | 79058 |
| rs769247388 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011440 | TGAATTCCCACCCCT[C/T]GGGGAAAGGCCCAGG | 79058 |
| rs769253755 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989227 | ATAAATATTAAATAA[A/G]TTTCTAAAAGCTCAG | 79058 |
| rs769288388 | snp | C/G | 0.000705965 | 0.0187746 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010004 | AAGCTCCGCCTCCCG[C/G]GTTCAAGTGGTTCTC | 79058 |
| rs769332145 | snp | A/G | 5.6802e-05 | 0.00532896 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994975 | GTCTCCAGGGCAGTG[A/G]CGGGAGACTCGGGCT | 79058 |
| rs769445335 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012847 | CAGGGTGAGGGTGCC[A/G]GGTTCCCAGCCCTGC | 79058 |
| rs769465239 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979192 | CCCCCAGGTTCTGGA[A/G]GACACGTGCCGGCGG | 79058 |
| rs769486667 | snp | C/T | 0.00017909 | 0.00946111 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015153 | CCAGAGCAGAGAACA[C/T]GCTTGCCAGTGGTAG | 79058 |
| rs769490804 | snp | C/G | 0.00071149 | 0.0188478 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008992 | CCCGGGGTGCGGAGG[C/G]CCCAGCCCGTGACAC | 79058 |
| rs769518097 | in-del | -/GTGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006212 | CTTGCATGTGCACAG[-/GTGT]GTGTGTGTGTGTGTG | 79058 |
| rs769520334 | snp | C/T | 2.96239e-05 | 0.00384852 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977704 | CTGGCCCCGAACGGC[C/T]GGCGCCACACGGTGA | 79058 |
| rs769534334 | snp | A/T | 1.75613e-05 | 0.00296316 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996818 | AGGAGCGGGAGCGGG[A/T]TCCCCAGCAGGAGCA | 79058 |
| rs769569943 | snp | C/T | 5.06975e-05 | 0.0050345 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017352 | AGGTGCCCACTCCGC[C/T]AGCCACAGGACCACC | 79058 |
| rs769592969 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004052 | CTCTGAGGTTGGGGC[C/T]ACCTCCGAATGGGTT | 79058 |
| rs769617882 | in-del | -/C | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017803 | CCCTGCAGCCAGCCT[-/C]CCCAGCAAGTCTGAT | 79058 |
| rs769746538 | snp | C/T | 2.24082e-05 | 0.00334718 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016761 | ATGGTGAGTGGACCC[C/T]TCCTCAGAGGCTCAG | 79058 |
| rs769780330 | snp | A/G | 2.1627e-05 | 0.00328832 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983666 | GAGGGGCCTGAGAAC[A/G]TGGTGGGTCGTGCTC | 79058 |
| rs769785909 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980503 | TGGGCTTTCTGCCCC[A/C]GACCTTCACACCATC | 79058 |
| rs769801455 | snp | A/G | 0.000131277 | 0.00810068 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016463 | GCCCCTGAGCCCCCC[A/G]CCCTCCCTGCAGGCG | 79058 |
| rs769808288 | snp | C/T | 1.66863e-05 | 0.0028884 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985486 | TTCCTAAGGAAGTTT[C/T]TCATGTCTTATACCC | 79058 |
| rs769829365 | snp | A/G | | | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012195 | ATGGGCGAGGTCCAC[A/G]GTGCTTCCTAACACG | 79058 |
| rs769854880 | in-del | -/AAAC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987869 | ACAAAAAAACAAAAG[-/AAAC]AACAAGGCTGGGCAC | 79058 |
| rs769884840 | snp | C/T | 0.000161499 | 0.00898461 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009481 | CCTTCCCCTCCTCAC[C/T]ACAGGAAGCGCCTGG | 79058 |
| rs769888805 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002965 | CTGCAACCTCCACCT[C/T]CTGGGTTCAAGCGAT | 79058 |
| rs769940753 | snp | G/T | 1.75072e-05 | 0.00295859 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015047 | TGCTCTGGCTGGGGG[G/T]ACGGTGTGACCCACT | 79058 |
| rs769941134 | in-del | -/AC | 3.66697e-05 | 0.00428176 | frameshift-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015113 | CCATTCACCCTGGGT[-/AC]CCCTCGCTGAAACGG | 79058 |
| rs769945901 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984194 | TTTTCTTTCTTTCTG[G/T]GGTCAGTTGTGCCTT | 79058 |
| rs769958810 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985443 | TCTGGAGAATCAGTC[C/T]GGGATTTAGAAGGAA | 79058 |
| rs770039721 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016574 | GTCCAGCCAGCCTGT[C/T]CCTGGACCTCAGAGC | 79058 |
| rs770064547 | snp | C/T | 1.87145e-05 | 0.00305891 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996381 | TGAGCCGGGGGTAGG[C/T]ACCACAAGGTGCTTC | 79058 |
| rs770115444 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997549 | TGGGCGTACAGTGGC[A/G]CGATCTCGGCTCACT | 79058 |
| rs770139209 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014384 | AGAAGGCAGGATGGC[C/T]CCTGCAGCCCCCACT | 79058 |
| rs770167654 | snp | A/C | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978352 | ACGGTGAAACCCCGT[A/C]TGTACTAAAAAAATA | 79058 |
| rs770171202 | snp | C/T | 2.73235e-05 | 0.00369608 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009215 | CCCCTCAGTGCCTCC[C/T]GGCATCTTCGCGCCA | 79058 |
| rs770182305 | snp | A/G | 5.00505e-05 | 0.00500227 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994790 | TTGAGCTGCCCTGGG[A/G]TACCTGATGGTTTCT | 79058 |
| rs770237371 | snp | A/G | 1.69887e-05 | 0.00291446 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996616 | GAGAAGCAGAGCACA[A/G]GGGCACCCGCAGCTG | 79058 |
| rs770264579 | snp | A/G | 1.67083e-05 | 0.00289031 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994855 | GGCGGGGCCACCCCA[A/G]TCTGCGTGTACACGA | 79058 |
| rs770278210 | snp | A/T | 1.67733e-05 | 0.00289592 | splice-acceptor-variant | ASPSCR1 | GRCh38.p7 | 17:82017307 | ATGTGTCTGCACTAC[A/T]GCCAGCAAGAGGTGA | 79058 |
| rs770307094 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999878 | GGGGCTCCCATCTAG[A/C]CCGGCGTCAGGGTCC | 79058 |
| rs770326672 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979398 | GCAGGGCCACACTCT[C/T]TCCAAATGCCCTAAG | 79058 |
| rs770330076 | snp | A/C | 1.73872e-05 | 0.00294844 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017034 | GGAGGGGGCGCTGGT[A/C]CCCCCTGAGCCCATC | 79058 |
| rs770359394 | snp | C/T | 2.73624e-05 | 0.00369871 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015066 | GTGTGACCCACTTTC[C/T]CTTTCCAGCCCCAGC | 79058 |
| rs770403645 | in-del | ACACACACCTGC/CACA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984854 | CCCTGCACACACCCC[ACACACACCTGC/CACA]ACACCCCCGCACACA | 79058 |
| rs770412362 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994475 | CCGTGAGCCGCATTC[C/T]GGAGCCAGTGCTGCT | 79058 |
| rs770414097 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008499 | GCTGCACGGCCCGGC[C/T]TTGTCAATTTCATTG | 79058 |
| rs770432298 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014301 | CCAACAGGCCCCCTT[C/T]CTTCCACCCACCAGG | 79058 |
| rs770504677 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989342 | CCCACGGTGAGGGTG[G/T]AGTGCCTGGTGGGCT | 79058 |
| rs770512994 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984003 | AGGACTACAGGTGCC[C/T]GCCACCACACCCGGC | 79058 |
| rs770548239 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006174 | TGGGTGCACGTGTGT[A/G]CACGGGTGTGTGTGT | 79058 |
| rs770570579 | snp | A/C/G | 6.71168e-05 | 0.00579263 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011515 | CGTGGTGGAAGAGCT[A/C/G]TCTGTATGTTCTTTT | 79058 |
| rs770630933 | snp | C/T | 2.45324e-05 | 0.00350222 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994965 | TCCCGCAGCCGTCTC[C/T]AGGGCAGTGGCGGGA | 79058 |
| rs770644643 | snp | A/G | 1.66073e-05 | 0.00288156 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011569 | CGAGACTTCGTGAGG[A/G]GCCACCTGGGGAACC | 79058 |
| rs770691166 | in-del | -/C | 3.46861e-05 | 0.00416435 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017034 | GGAGGGGGCGCTGGT[-/C]CCCCCTGAGCCCATC | 79058 |
| rs770730578 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005084 | CAGCCGTGGGGCTCT[C/T]GCCTCTGCCAGAGCA | 79058 |
| rs770752712 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012935 | CTGCCTGGGGCCTTC[C/T]GAAGCCCTCTGGCCT | 79058 |
| rs770770974 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982529 | CTATCCTGTCTTGAC[A/G]TAGACATTTCATGTG | 79058 |
| rs770795341 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992796 | AAATCCAAGGCCCTT[C/T]GTTGGCTGCTCTGTG | 79058 |
| rs770799898 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992205 | GGCCCTGGGTCTTGC[C/G]CCTGCGGACATTGGG | 79058 |
| rs770847900 | snp | C/T | 0.000141093 | 0.00839803 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016457 | CACCCGGCCCCTGAG[C/T]CCCCCGCCCTCCCTG | 79058 |
| rs770951126 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981984 | TTTTTCTTTCTTTTT[C/T]TTGAGACGGAGTCTC | 79058 |
| rs770951802 | in-del | -/GGC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005324 | CTCGGAGGCCTGCGG[-/GGC]AGTGGTCCCCCGGCT | 79058 |
| rs770952288 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016671 | AGTAACCACCTCCCC[A/G]AGAGAGGACTGGGAC | 79058 |
| rs771126369 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005201 | GGGCAGTCCTGGCCC[A/G]CTGGGCAGAGCAGAA | 79058 |
| rs771144457 | snp | C/T | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017715 | GTCACCCCACATCCG[C/T]AGGGCAGGGCCTGGC | 79058 |
| rs771150836 | snp | G/T | 1.66905e-05 | 0.00288876 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994772 | GGGCCTCCGTGGCAC[G/T]GGTTGAGCTGCCCTG | 79058 |
| rs771160269 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986445 | AAAAAATAAATAAAT[A/G]AAAATAAGTAATTGA | 79058 |
| rs771189046 | snp | C/T | 2.37719e-05 | 0.00344752 | splice-donor-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009193 | CTCAAGAGTGAGCGG[C/T]GGGTGCCCCCTCAGT | 79058 |
| rs771264158 | snp | A/G | 1.68252e-05 | 0.0029004 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016957 | TACATGTCCAGGGCC[A/G]CCGGGTCCCCTTCCC | 79058 |
| rs771325005 | snp | C/T | 1.67475e-05 | 0.00289369 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016898 | GGTCTGGGGGCACCT[C/T]CCGTGGCGGCACTCA | 79058 |
| rs771334750 | in-del | -/ACCA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986300 | ATAGTGCATGGTGGT[-/ACCA]GCGTGCCTGTGGTCC | 79058 |
| rs771354917 | in-del | -/AGCAGG | 0.000393947 | 0.0140292 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996788 | CGGGCCAGGATCCCC[-/AGCAGG]AGCAGGAGCAGGAGC | 79058 |
| rs771369911 | snp | C/T | 1.66446e-05 | 0.00288479 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010785 | GTCCCTCCAACCCTT[C/T]CACTTGTCTGGCCTA | 79058 |
| rs771454611 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999880 | GGCTCCCATCTAGCC[C/T]GGCGTCAGGGTCCAG | 79058 |
| rs771509644 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997662 | CCAGCTAATTTTTTT[-/A]GTATTTTTAGTAGAG | 79058 |
| rs771528983 | snp | A/T | 1.74909e-05 | 0.00295722 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017040 | GGCGCTGGTCCCCCC[A/T]GAGCCCATCCCAGGG | 79058 |
| rs771650282 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002383 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTGA | 79058 |
| rs771709282 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983776 | AAGGAGGGACATGAG[G/T]CTTAGCACCAGTTCT | 79058 |
| rs771724909 | snp | G/T | 1.82417e-05 | 0.00302002 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983583 | TGCTCGACCTTTCTC[G/T]CCAGTGGAGATTTGC | 79058 |
| rs771732182 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007571 | CTGAGCACGGCATGT[C/T]CTGGGGCCCCGTCTG | 79058 |
| rs771769700 | snp | A/G/T | 5.02873e-05 | 0.00501414 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996690 | CCCTCCTGGGCCCAC[A/G/T]AGGCCTCTGACATCA | 79058 |
| rs771809671 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990257 | ACCTGCATGTATGGT[A/G]CACTTGGAGCATCTC | 79058 |
| rs771820817 | snp | G/T | 1.68411e-05 | 0.00290177 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011495 | CTGGGGCAGCCCGGG[G/T]CTGGCGTGGTGGAAG | 79058 |
| rs771889026 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001178 | CTGGGCCTGGAGCGG[G/T]TCATGCACTGGGCGT | 79058 |
| rs771918768 | in-del | -/ATTTT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002251 | CATCTTTTCATTTTC[-/ATTTT]ATTTTATTTTATTTT | 79058 |
| rs771921352 | snp | A/C/G/T | 6.59877e-05 | 0.00574374 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979291 | TATCTGTGCCCCTGC[A/C/G/T]CCCTGAACATACTGG | 79058 |
| rs771928252 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982602 | AAGTTTGTTCTCTCT[C/T]AATTCTTCCAGATGC | 79058 |
| rs771976450 | snp | C/T | 2.37408e-05 | 0.00344527 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995986 | TCCTGGCTGCTCCTC[C/T]TGCAGGTGACGGGTG | 79058 |
| rs771991354 | snp | C/T | 3.82351e-05 | 0.00437219 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009019 | ACACCCGCCGTCAGC[C/T]GCGCCCTCTGCCTCC | 79058 |
| rs772041819 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983253 | CTCTCTGTGTTTTCC[A/G]AGCGTCTGCACTGGG | 79058 |
| rs772075889 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006407 | TGTTTGCCCCAGAGC[A/G]GAAGGAAAGTGAATG | 79058 |
| rs772079890 | snp | G/T | 4.93012e-05 | 0.00496469 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009102 | CCTGGAGGAGCGGCT[G/T]CAGGCCTGGCCAGCG | 79058 |
| rs772085653 | snp | G/T | 1.74983e-05 | 0.00295784 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017382 | CTCCTCTGCCAGCAG[G/T]AATAAAGACTTGTGC | 79058 |
| rs772117213 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015022 | TCCCTCAAAGGCCCT[C/T]CCCGGGCCCTGCTCT | 79058 |
| rs772136712 | snp | A/G | 0.000137115 | 0.00827882 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012176 | TCTTCCTTCGGGCGC[A/G]TGGATGGGCGAGGTC | 79058 |
| rs772139525 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014556 | GAGGCACTGTGGTGC[C/T]GCCTTCCTCCCGGGC | 79058 |
| rs772181461 | snp | A/G | 5.67408e-05 | 0.00532609 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012110 | GCACAGGGCGTGCTC[A/G]TGAGGGGCTCTTCTG | 79058 |
| rs772193481 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006278 | GTGTGCGTGTCCTTG[C/T]GGGTGCACGTGCGTG | 79058 |
| rs772214131 | in-del | -/GGAGCGGGAGCGGGATCCCCAGCAGGAGCAGGAGCG | 1.73292e-05 | 0.00294352 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996804 | GCAGGAGCAGGAGCA[lengthTooLong]GGAGCGGGTAAAAGG | 79058 |
| rs772223567 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012491 | TCTGCTTCCTGCCTG[G/T]CCCCGGGTGGGAAAG | 79058 |
| rs772283247 | snp | A/G | 1.72677e-05 | 0.00293829 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996541 | GGGGAGCTCAGCCGC[A/G]GCGACTTGAGCCGTC | 79058 |
| rs772297023 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976127 | AGCCACGGACCTTGA[A/C]CATGGAGGAATTCAG | 79058 |
| rs772345307 | snp | A/G | 1.66197e-05 | 0.00288263 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985498 | TTTCTCATGTCTTAT[A/G]CCCTCCAGGTTCGCA | 79058 |
| rs772359070 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997280 | GTCACATTTACATCC[A/T]CTCAACTACATGCAC | 79058 |
| rs772416540 | snp | A/G | 1.67942e-05 | 0.00289772 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016945 | CCTCCCCACAGGTAC[A/G]TGTCCAGGGCCGCCG | 79058 |
| rs772474840 | snp | C/T | 7.17798e-05 | 0.00599039 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015138 | AAACGGTGCCTGGGA[C/T]CAGAGCAGAGAACAC | 79058 |
| rs772474935 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980298 | GAAGACCTGTTTTTA[C/T]AGTACTGTTGTCCTA | 79058 |
| rs772541356 | snp | A/T | 0.000448732 | 0.0149721 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009918 | TTAGAATGAAACCTT[A/T]TTTTTTTTTTGAGAC | 79058 |
| rs772593156 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012869 | CAGCCCTGCTGGGCC[A/G]CCCTCCAGAGCCAGA | 79058 |
| rs772651350 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999375 | CTCACACCTGTAATC[C/G]CAGCAGTTTGGGAGA | 79058 |
| rs772665324 | snp | A/G | 1.64855e-05 | 0.00287097 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979153 | AGCCCTGCACACTCA[A/G]CAGTTCACCATCCTT | 79058 |
| rs772676675 | snp | C/T | 1.66513e-05 | 0.00288537 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012299 | GTACCTGAGGGCCTC[C/T]CTGGGGTGCTGCGGG | 79058 |
| rs772676735 | snp | A/G | 2.22403e-05 | 0.00333461 | intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017121 | GCTGCCGGGTACTGC[A/G]GCTGGGTGGAAGGTG | 79058 |
| rs772718306 | snp | C/G | 0.000462856 | 0.0152057 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977686 | GGCTCCGCGGTGTCG[C/G]TGCTGGCCCCGAACG | 79058 |
| rs772729531 | snp | G/T | 3.50128e-05 | 0.00418392 | stop-gained, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017041 | GCGCTGGTCCCCCCT[G/T]AGCCCATCCCAGGGA | 79058 |
| rs772810332 | snp | A/G | 1.69453e-05 | 0.00291073 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994883 | CGAGGGATGAGGTAG[A/G]CGGCCTGCTCTTGCT | 79058 |
| rs772817804 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991395 | GTGGCTCCGGGAAAG[C/G]TGGGTGATTTCTGCA | 79058 |
| rs772863497 | snp | C/T | 1.6659e-05 | 0.00288604 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994811 | GATGGTTTCTTTCCT[C/T]TCCTCCCAGGGAGTG | 79058 |
| rs772870857 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986816 | CTGCTCCCGTCTGAC[A/G]GTAGTGCCGCGCTGC | 79058 |
| rs772901549 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999739 | CCGGAACTCAGGTGA[G/T]GTCAGGAGTTTGCTT | 79058 |
| rs772904862 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004215 | GTTTCCCAGCTCAGC[A/G]GCCCAGGGATGCCCC | 79058 |
| rs772924711 | snp | C/T | 1.81099e-05 | 0.00300909 | stop-gained, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983585 | CTCGACCTTTCTCTC[C/T]AGTGGAGATTTGCCA | 79058 |
| rs772927018 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002530 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCTCTG | 79058 |
| rs772964503 | snp | A/T | 1.7894e-05 | 0.0029911 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015267 | CCATGCCACCCAGTC[A/T]GCCGACCCTCCTCTC | 79058 |
| rs773030214 | in-del | -/AG | 2.54644e-05 | 0.00356813 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015399 | CACAGAGGCGCAGAC[-/AG]GGAGCCCAGGTGCCC | 79058 |
| rs773070452 | snp | C/T | 0.000101542 | 0.00712464 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996634 | GCACCCGCAGCTGCC[C/T]CCTTTGTTCCTTTCT | 79058 |
| rs773070766 | in-del | -/CA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992401 | CCTCTGGAGGAGCCG[-/CA]CACATCAAAGCCGGG | 79058 |
| rs773106245 | snp | A/C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990806 | ATTGTTATGCTAACG[A/C/G]GTTTCCTATGAGGAG | 79058 |
| rs773120026 | snp | A/G | 0.000876878 | 0.0209206 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009114 | GCTGCAGGCCTGGCC[A/G]GCGGAGCTGCCTGAT | 79058 |
| rs773192312 | in-del | -/CTTTGATCTGGGA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000389 | TGGCGTGCTGAGGGC[-/CTTTGATCTGGGA]CTTGGGCAGCTGATT | 79058 |
| rs773204104 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984385 | GAGTTTGGGACCAGC[C/T]GGCCAACATAATGAA | 79058 |
| rs773244022 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981789 | TTATTGTGCCTCAGC[A/G]TCTTGAGTAGCTGGA | 79058 |
| rs773266415 | snp | A/G | 1.80309e-05 | 0.00300252 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015319 | GTGGCGATCCCTCCC[A/G]AGTCAAGGCTGGGCA | 79058 |
| rs773293816 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980513 | GCCCCAGACCTTCAC[A/C]CCATCCTTCTCCAGT | 79058 |
| rs773295243 | snp | C/T | 1.65605e-05 | 0.0028775 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995943 | AGGGCTTCCCTGGGC[C/T]CTGGGGTCCCGGTGC | 79058 |
| rs773350181 | snp | C/T | 0.00113443 | 0.0237892 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009021 | ACCCGCCGTCAGCCG[C/T]GCCCTCTGCCTCCAG | 79058 |
| rs773447631 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997556 | ACAGTGGCGCGATCT[C/T]GGCTCACTGCAGCCT | 79058 |
| rs773457089 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995318 | GGAGGGGCCCTGGGG[A/G]GCCAGGACATTCCCC | 79058 |
| rs773467041 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016605 | CAGCTGCCCGGGAGG[A/G]CGTTCGGTCTGGGGC | 79058 |
| rs773535524 | in-del | -/GCTCCGGGATGAGGCCGTGTGG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997105 | GATGAGGCCGTGTCC[-/GCTCCGGGATGAGGCCGTGTGG]GCTCCGGGATGAGGC | 79058 |
| rs773629177 | snp | C/T | 5.55448e-05 | 0.00526966 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012118 | CGTGCTCGTGAGGGG[C/T]TCTTCTGCCCCACTT | 79058 |
| rs773688749 | snp | A/C | 1.6588e-05 | 0.00287988 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985571 | TCTGTTCAGGCCAGA[A/C]CCTCTGGGAGCTTCT | 79058 |
| rs773710535 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007443 | CCCCCATCCTGGAGG[C/T]ACCCTGGTGTGGGCT | 79058 |
| rs773765956 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016338 | AGACAGGAAGCTGGG[C/T]GATGGGCTCATGGGG | 79058 |
| rs773771627 | snp | A/G | 0.000149914 | 0.00865647 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009950 | GAGTCTCTCTCTGTC[A/G]CCCAGGCTGGAGTCA | 79058 |
| rs773820877 | snp | A/G | 1.68318e-05 | 0.00290096 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016960 | ATGTCCAGGGCCGCC[A/G]GGTCCCCTTCCCCAT | 79058 |
| rs773847070 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987867 | AAACAAAAAAACAAA[A/G]GAAACAACAAGGCTG | 79058 |
| rs773864878 | snp | A/G | 1.69902e-05 | 0.00291458 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996619 | AAGCAGAGCACAAGG[A/G]CACCCGCAGCTGCCC | 79058 |
| rs773890482 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014385 | GAAGGCAGGATGGCT[C/T]CTGCAGCCCCCACTC | 79058 |
| rs773905181 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994491 | GGAGCCAGTGCTGCT[C/T]GCCCCTCCTGTGCGG | 79058 |
| rs773925812 | snp | C/T | 1.64955e-05 | 0.00287184 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979284 | CTGAGTATATCTGTG[C/T]CCCTGCCCCCTGAAC | 79058 |
| rs773931593 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016600 | AGAGCCAGCTGCCCG[G/T]GAGGGCGTTCGGTCT | 79058 |
| rs774003805 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011676 | GTGGGCACACCGCCC[A/G]TCCCAGCTGGGGCTC | 79058 |
| rs774044426 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992244 | AGGTCTGCGTGGGGG[A/C]GGGGGAGTAGGGGCT | 79058 |
| rs774092162 | snp | G/T | 2.53078e-05 | 0.00355714 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995975 | AGGCGCACCTGTCCT[G/T]GCTGCTCCTCCTGCA | 79058 |
| rs774097823 | snp | C/G | 1.68159e-05 | 0.0028996 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017330 | AGAGGTGAGAGCTGC[C/G]AGCCTGAGGTGCCCA | 79058 |
| rs774149159 | snp | C/T | 9.88533e-05 | 0.00702971 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995096 | GTTTTTTCAGCTTCT[C/T]TCAAAGCCCAAGAGT | 79058 |
| rs774213125 | snp | G/T | 1.66374e-05 | 0.00288417 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010821 | CTCTGAGGGTCCTGT[G/T]CCCCGACCGCTACGT | 79058 |
| rs774233711 | snp | C/T | 1.72193e-05 | 0.00293417 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017375 | GGACCACCTCCTCTG[C/T]CAGCAGGAATAAAGA | 79058 |
| rs774266642 | snp | C/T | 1.78851e-05 | 0.00299036 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015242 | AGCCTCTCCAAGCAC[C/T]GGTCAGCCTCCATGC | 79058 |
| rs774273592 | snp | C/T | 1.67928e-05 | 0.0028976 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011651 | CTCCAGTGCTCGGGG[C/T]CTTGGTGCTGTGGGC | 79058 |
| rs774319865 | snp | A/G | 1.78953e-05 | 0.00299121 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015177 | GTGGTAGGAGATGGA[A/G]GCGACGTGGACTCTG | 79058 |
| rs774341591 | snp | C/T | 7.07489e-05 | 0.00594722 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994985 | CAGTGGCGGGAGACT[C/T]GGGCTCTTGAAAGCA | 79058 |
| rs774353864 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982536 | GTCTTGACGTAGACA[C/T]TTCATGTGGCAATTT | 79058 |
| rs774388888 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012976 | TCTTCAAAGCCTCTT[C/G]AGATATTTTAATTAG | 79058 |
| rs774394455 | snp | C/T | 5.4076e-05 | 0.00519953 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996838 | CAGCAGGAGCAGGAG[C/T]GGGAGCGGGTAAAAG | 79058 |
| rs774425226 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016674 | AACCACCTCCCCGAG[A/G]GAGGACTGGGACAGC | 79058 |
| rs774550098 | snp | A/G | 2.07428e-05 | 0.0032204 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016490 | GGCGAACCTCTTCCC[A/G]GCCGCTCTGGTGCAC | 79058 |
| rs774574305 | snp | C/T | 2.00114e-05 | 0.00316312 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016784 | AGGCTCAGGGTGAGC[C/T]TGGGCCTCCCTGCAG | 79058 |
| rs774585037 | snp | C/G | 7.04399e-05 | 0.00593422 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009503 | AGCGCCTGGAAGAAG[C/G]CCCCTTGGTGACCAA | 79058 |
| rs774654669 | in-del | -/TTTTTTTTTTTTTTTTTTTTTCTGGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997487 | TTTTTTTTTTCTGGG[-/TTTTTTTTTTTTTTTTTTTTTCTGGT]TTTTTTTTTTTTTTT | 79058 |
| rs774678478 | snp | A/G | 6.87805e-05 | 0.00586392 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996474 | AGGAAGCCTGGGCTC[A/G]TCAGCGTCGGCTGGC | 79058 |
| rs774686048 | in-del | -/AGCAGGAGCAGGAGCGGGAGCGGGATCCCC | 6.89982e-05 | 0.00587319 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996794 | AGGATCCCCAGCAGG[lengthTooLong]AGCAGGAGCAGGAGC | 79058 |
| rs774709296 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995375 | TGGCTGGGGCTGTGA[C/T]GGGGAGGTTCAGGTC | 79058 |
| rs774802736 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015516 | GGTTGGGGGTCCTGG[C/T]CTGTGGGGGCTATGA | 79058 |
| rs774852840 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990267 | ATGGTGCACTTGGAG[C/T]ATCTCGGTCTGGGCC | 79058 |
| rs774864875 | snp | A/G | 0.00056899 | 0.0168574 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010011 | GCCTCCCGGGTTCAA[A/G]TGGTTCTCCTGCCTC | 79058 |
| rs774894770 | snp | C/T | 5.89779e-05 | 0.00543005 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015061 | GGACGGTGTGACCCA[C/T]TTTCCCTTTCCAGCC | 79058 |
| rs774961866 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986479 | GTATCAGTTTCTGTC[A/G]GTTAATGGTTTAAAC | 79058 |
| rs774997854 | snp | A/C | 1.6477e-05 | 0.00287024 | missense, intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979195 | CCAGGTTCTGGAGGA[A/C]ACGTGCCGGCGGCAG | 79058 |
| rs775012345 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979670 | ATCTTTTTTGGGGGG[A/G]CCACCATTCAACCCC | 79058 |
| rs775015648 | snp | A/G | 3.32851e-05 | 0.00407939 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010787 | CCCTCCAACCCTTCC[A/G]CTTGTCTGGCCTAGG | 79058 |
| rs775017122 | in-del | -/CT | | | intron-variant, utr-variant-5-prime | ASPSCR1 | GRCh38.p7 | 17:81981288 | AGCCATGGCCAGGAA[-/CT]CAGCTTTCAAGGTTT | 79058 |
| rs775022790 | in-del | -/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997675 | TTTGTATTTTTAGTA[-/G]AGACAGGGTTTTACC | 79058 |
| rs775043095 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007613 | CAGTACGAGCCCATC[A/T]GGGGTACTCTGCCCG | 79058 |
| rs775051241 | snp | C/T | 2.5602e-05 | 0.00357775 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995055 | GGAGCCCGGGCTGCC[C/T]CGAAACCTCCCTCGG | 79058 |
| rs775168320 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002483 | TGGTCTCGCACTCCT[A/G]ACCTCAGGTGATCCA | 79058 |
| rs775200193 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985368 | GAATAGGAGGGTAGC[C/T]TTCTCCGTGGGGGTC | 79058 |
| rs775205923 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007347 | GGATCCACAGGAATT[-/A]AGAGATTTTTTCAGT | 79058 |
| rs775253047 | snp | C/G | 0.000631114 | 0.0177527 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977729 | CGGTGAAGGTGACGC[C/G]GAGCACCGTGCTGCT | 79058 |
| rs775277411 | snp | A/T | 1.7581e-05 | 0.00296483 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996819 | GGAGCGGGAGCGGGA[A/T]CCCCAGCAGGAGCAG | 79058 |
| rs775397832 | snp | A/G | 1.67916e-05 | 0.0028975 | synonymous-codon, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017321 | CAGCCAGCAAGAGGT[A/G]AGAGCTGCCAGCCTG | 79058 |
| rs775411504 | snp | C/T | 2.23321e-05 | 0.00334149 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016763 | GGTGAGTGGACCCCT[C/T]CTCAGAGGCTCAGGG | 79058 |
| rs775450756 | snp | G/T | 0.000121979 | 0.00780864 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017152 | GGGTGCTGTGGCCGG[G/T]TGGAGGGCGGGGGTC | 79058 |
| rs775471582 | snp | A/C | 3.31939e-05 | 0.0040738 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82011583 | GAGCCACCTGGGGAA[A/C]CCCGAGCTGTCATTT | 79058 |
| rs775471779 | snp | C/T | 1.68111e-05 | 0.00289918 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996731 | AGTTGCCGAAGTCCC[C/T]CTCCAGCCCTGGAGG | 79058 |
| rs775524594 | snp | C/T | 1.67351e-05 | 0.00289263 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011524 | AGAGCTGTCTGTATG[C/T]TCTTTTTCTCCTCTG | 79058 |
| rs775570441 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006346 | GCTTGGGTGCATGCA[C/G]GTGTGTGTGTATATG | 79058 |
| rs775586464 | in-del | -/A | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991889 | GAGAGCTCTAGACTC[-/A]ACTGCCTTGTCCCCA | 79058 |
| rs775614268 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82001192 | GGTCATGCACTGGGC[A/G]TGGTGAATACACCCT | 79058 |
| rs775653566 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982603 | AGTTTGTTCTCTCTT[A/T]ATTCTTCCAGATGCC | 79058 |
| rs775666841 | snp | A/G | 5.47795e-05 | 0.00523324 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009216 | CCCTCAGTGCCTCCC[A/G]GCATCTTCGCGCCAG | 79058 |
| rs775704771 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982214 | CCTCAAGTGATCTGC[C/T]CGTCTGGGCCTCCCA | 79058 |
| rs775722307 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012286 | GACCCTCTTTCAGGT[A/G]CCTGAGGGCCTCCCT | 79058 |
| rs775726879 | snp | C/T | 1.86872e-05 | 0.00305667 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996383 | AGCCGGGGGTAGGCA[C/T]CACAAGGTGCTTCCC | 79058 |
| rs775731936 | in-del | -/GGAGCGGGATCCCCAGCAGGAGCA | 1.74224e-05 | 0.00295142 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996810 | GCAGGAGCAGGAGCG[-/GGAGCGGGATCCCCAGCAGGAGCA]GGAGCGGGAGCGGGT | 79058 |
| rs775743381 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993195 | AGGGAGGCAAGTCCT[G/T]CCCTTTTTTTTGTTT | 79058 |
| rs775761036 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985614 | ACAGATCAGGTGAGC[A/C]TCAGTGGGCTGGGGG | 79058 |
| rs775766042 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010495 | GATCATGCCACTGCA[C/G]TCCAGCCTGGGCGAC | 79058 |
| rs775838835 | snp | A/G | 1.76033e-05 | 0.00296671 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983609 | TTTGCCAACCTGCCC[A/G]ACAATGCCAAGCTGG | 79058 |
| rs775850096 | snp | A/G | 7.71456e-05 | 0.00621022 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009488 | CTCCTCACCACAGGA[A/G]GCGCCTGGAAGAAGC | 79058 |
| rs775988018 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980446 | CTTGTGTCTGGACCA[C/T]GTGAGAATCCCAGGA | 79058 |
| rs776037647 | snp | C/T | 1.73845e-05 | 0.00294821 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017036 | AGGGGGCGCTGGTCC[C/T]CCCTGAGCCCATCCC | 79058 |
| rs776087782 | snp | A/G | 2.34414e-05 | 0.00342347 | intron-variant, splice-donor-variant | ASPSCR1 | GRCh38.p7 | 17:82017134 | GCGGCTGGGTGGAAG[A/G]TGGGGTGCTGTGGCC | 79058 |
| rs776101192 | snp | A/G | 3.3315e-05 | 0.00408122 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009531 | CAAGGCCTTCAGGGA[A/G]GCGCAGATAAAGGAG | 79058 |
| rs776107844 | snp | A/G | 1.66682e-05 | 0.00288684 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994799 | CCTGGGGTACCTGAT[A/G]GTTTCTTTCCTCTCC | 79058 |
| rs776111496 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008826 | GGGGGGTCTCCAGCC[C/G]TGGACAGGCTCTGAG | 79058 |
| rs776117695 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82004403 | CCTTGGCGGCCCTCC[C/T]GGAGGCCGGGACCTG | 79058 |
| rs776180763 | snp | A/G | 1.79342e-05 | 0.00299445 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015141 | CGGTGCCTGGGACCA[A/G]AGCAGAGAACACGCT | 79058 |
| rs776182994 | snp | C/T | 7.00415e-05 | 0.00591742 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996814 | GAGCAGGAGCGGGAG[C/T]GGGATCCCCAGCAGG | 79058 |
| rs776213573 | snp | C/G | 0.000510074 | 0.0159617 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977697 | GTCGGTGCTGGCCCC[C/G]AACGGCCGGCGCCAC | 79058 |
| rs776242741 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979762 | GGCCGTGGAGAAATA[A/G]GATGCCTTGAAAACT | 79058 |
| rs776281779 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976504 | GACATGGATATGTCA[C/T]CGACAGGAAGGCACA | 79058 |
| rs776306980 | snp | A/G | 1.78931e-05 | 0.00299102 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015183 | GGAGATGGAGGCGAC[A/G]TGGACTCTGGGAGGC | 79058 |
| rs776315690 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991236 | GTGCTGGCGTGGGCA[C/T]CCCAGGTGGGAGTGG | 79058 |
| rs776409069 | snp | A/G | 2.63647e-05 | 0.00363066 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994968 | CGCAGCCGTCTCCAG[A/G]GCAGTGGCGGGAGAC | 79058 |
| rs776435936 | snp | C/T | 3.34879e-05 | 0.0040918 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996707 | GGCCTCTGACATCAT[C/T]TTCAGCTAAGTTGCC | 79058 |
| rs776459610 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010391 | AAAATTAGTCAGGAG[A/T]GGTGGCGCACGCCTG | 79058 |
| rs776493319 | snp | C/G | 3.35464e-05 | 0.00409537 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010874 | AGCGAGACAGGTGGG[C/G]AGCGCTGTGGGGTGT | 79058 |
| rs776566478 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002718 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 79058 |
| rs776611658 | snp | C/T | 0.000272368 | 0.0116666 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016460 | CCGGCCCCTGAGCCC[C/T]CCGCCCTCCCTGCAG | 79058 |
| rs776613347 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989892 | TCCCGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC | 79058 |
| rs776656737 | snp | A/G | 1.92435e-05 | 0.00310184 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015352 | AGCACGTGGGGACAG[A/G]CCGGGTAGGCTGCCT | 79058 |
| rs776685313 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982700 | AACCACTTTGAGTAT[A/G]TTCAGATTTTTCTTT | 79058 |
| rs776709237 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994429 | GCCCAGACGTCGGTA[C/T]CCTGACTCTCAGGCT | 79058 |
| rs776729456 | in-del | -/GGG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006097 | TGCACGTGTGTGCTT[-/GGG]GGCGTGTGTGTGTCC | 79058 |
| rs776731631 | snp | A/G | 3.32873e-05 | 0.00407953 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983507 | CGTGGATGGCAGGGC[A/G]TGTCAGGCTCTGCAG | 79058 |
| rs776774074 | in-del | -/G | 1.78868e-05 | 0.0029905 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996834 | TCCCCAGCAGGAGCA[-/G]GAGCGGGAGCGGGTA | 79058 |
| rs776784908 | snp | A/C/G | 0.000222734 | 0.0105509 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996008 | TGACGGGTGAAGCTG[A/C/G]CCTGCGGGGCACGAC | 79058 |
| rs776860647 | snp | A/T | 2.54191e-05 | 0.00356495 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009206 | GGTGGGTGCCCCCTC[A/T]GTGCCTCCCGGCATC | 79058 |
| rs776895015 | snp | A/C/T | 5.04658e-05 | 0.00502303 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016958 | ACATGTCCAGGGCCG[A/C/T]CGGGTCCCCTTCCCC | 79058 |
| rs776949086 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014624 | GCCTCCCTCCCGGGC[A/G]TCTTGAGCTGCAAGG | 79058 |
| rs777018835 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987641 | ATTGTGGTAGCATAA[A/G]CCTCTTCAACAGACT | 79058 |
| rs777044798 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005639 | TCCCCGCTGGCCCTC[C/T]GTCTGCTTGGGAGCT | 79058 |
| rs777047867 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006402 | ATGCATGTTTGCCCC[A/C]GAGCGGAAGGAAAGT | 79058 |
| rs777104948 | snp | A/C | 1.65765e-05 | 0.00287888 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81985547 | ATGGCTCGAGGTTGC[A/C]GGACTCTTTCTGTTC | 79058 |
| rs777110091 | snp | C/G | 1.67164e-05 | 0.00289101 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012192 | TGGATGGGCGAGGTC[C/G]ACGGTGCTTCCTAAC | 79058 |
| rs777141234 | snp | C/T | 1.67517e-05 | 0.00289406 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016900 | TCTGGGGGCACCTCC[C/T]GTGGCGGCACTCACC | 79058 |
| rs777163081 | snp | C/T | 2.6475e-05 | 0.00363824 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012129 | GGGGCTCTTCTGCCC[C/T]ACTTGAGGCGTCACC | 79058 |
| rs777196112 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981400 | TTATTATTTTTTGAG[A/G]TGGAGTCTCGCTCTG | 79058 |
| rs777251985 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007780 | AACCCAGGCGTGCTC[A/G]CGGCCCTCTGGAATG | 79058 |
| rs777307133 | in-del | -/GC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006101 | CGTGTGTGCTTGGGG[-/GC]GTGTGTGTGTCCTTG | 79058 |
| rs777308203 | in-del | -/CT | 0.00316175 | 0.0396343 | frameshift-variant, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017039 | GGGCGCTGGTCCCCC[-/CT]GAGCCCATCCCAGGG | 79058 |
| rs777370460 | snp | A/C | 0.00010634 | 0.00729099 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983718 | GGCACAGGATCGTTC[A/C]GCTGGCCAGGGACGG | 79058 |
| rs777380473 | snp | A/G | | | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996793 | CAGGATCCCCAGCAG[A/G]AGCAGGAGCAGGAGC | 79058 |
| rs777400561 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982497 | CAGCCTGCCTGCCCT[C/T]GGGATCCCCCGATCT | 79058 |
| rs777406142 | snp | A/G | 0.000155775 | 0.00882403 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016437 | GCAGGGGGGTGCTCT[A/G]CCCACACCCGGCCCC | 79058 |
| rs777424441 | snp | C/T | 3.86354e-05 | 0.00439502 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983648 | CCCGCTTCCCGGAGC[C/T]GTGAGGGGCCTGAGA | 79058 |
| rs777532319 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013978 | CACGGTCACCTCACT[A/T]ATCTCTTCAAAGGCT | 79058 |
| rs777556431 | snp | C/G | 3.48791e-05 | 0.00417592 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009443 | CTGTTGCCAGGGCCC[C/G]CATTCTGACCAGAAG | 79058 |
| rs777570296 | snp | C/T | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017634 | CTTGAGGAAAGTCTT[C/T]TGGGGGAAATCACCT | 79058 |
| rs777593926 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975851 | TCACTGCGAGCTCTG[C/T]CTCCCGGATTCACGC | 79058 |
| rs777681439 | snp | G/T | | | upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977503 | AAGGGCGGGGCCGGG[G/T]CGCCGTGGGTGGGGA | 79058 |
| rs777751249 | snp | C/T | 6.39284e-05 | 0.00565333 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996032 | GCACGACGCTGCAGT[C/T]GCTGGGCCTGACCGG | 79058 |
| rs777781709 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013827 | CAAAGCCCCCCGCCC[C/T]TGCCTGAAACCTGCG | 79058 |
| rs777824886 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81992174 | GGTGGCTTGGCCTGG[C/T]CTGGGGTCCCCGGGA | 79058 |
| rs777847277 | snp | A/G | 5.00104e-05 | 0.00500027 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994840 | TGCCTGCAGCACCCC[A/G]GCGGGGCCACCCCAG | 79058 |
| rs777852943 | snp | C/T | 1.70487e-05 | 0.0029196 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985635 | GGGCTGGGGGCTCTT[C/T]CCTACCCTGTTTGCT | 79058 |
| rs777900951 | snp | G/T | 1.67158e-05 | 0.00289096 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012332 | GGGGCCCTCCAGGGA[G/T]GGCAGGACGAGAGCG | 79058 |
| rs777946155 | snp | A/G | 6.64176e-05 | 0.00576233 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012260 | AAAACAGTCCTGGAC[A/G]ACCACACGCAGACCC | 79058 |
| rs777947717 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990984 | GCCAAGTGGTGAAAG[G/T]CAGGGGTGTGGATGG | 79058 |
| rs778008232 | in-del | -/CACA | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985230 | AACTGCACACCCCCG[-/CACA]CACACACCCACACAC | 79058 |
| rs778009080 | snp | A/G | 1.71971e-05 | 0.00293227 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017023 | CCAGCTGCTGAGGAG[A/G]GGGCGCTGGTCCCCC | 79058 |
| rs778014797 | snp | A/G | 1.70831e-05 | 0.00292254 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996593 | GGCCCTGCTGCGAGC[A/G]CACTCAGGAGAAGCA | 79058 |
| rs778090323 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81979445 | CTCTTCCAGCTTCTC[A/T]TGGCTCCAAGCGTTC | 79058 |
| rs778120965 | snp | A/G | 0.00029968 | 0.0122373 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010779 | CCGGCCGTCCCTCCA[A/G]CCCTTCCACTTGTCT | 79058 |
| rs778158732 | in-del | -/CAGCAG | 5.1329e-05 | 0.00506575 | cds-indel, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996787 | TCGGGCCAGGATCCC[-/CAGCAG]GAGCAGGAGCAGGAG | 79058 |
| rs778194480 | snp | C/G | 1.6808e-05 | 0.00289892 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016949 | CCCACAGGTACATGT[C/G]CAGGGCCGCCGGGTC | 79058 |
| rs778213782 | snp | C/T | 1.78889e-05 | 0.00299068 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015217 | TTTTTTGGGGTCCAT[C/T]CAGAGGCCGAGCCTC | 79058 |
| rs778307638 | snp | A/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014493 | ACCTCCCTCCCAGAC[A/T]CCATGATGCTGCCTC | 79058 |
| rs778321620 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980179 | GTAGAGATGGGGTTT[C/T]ACCACATTGGCCAGG | 79058 |
| rs778337977 | snp | C/T | 1.86886e-05 | 0.00305679 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983641 | GATGGTGCCCGCTTC[C/T]CGGAGCCGTGAGGGG | 79058 |
| rs778381380 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986461 | AAAATAAGTAATTGA[C/T]GTGTATCAGTTTCTG | 79058 |
| rs778388667 | snp | C/T | 1.64789e-05 | 0.0028704 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979255 | GTGAGTTTGCTCCAG[C/T]TCAGCAGCAGGGTCT | 79058 |
| rs778395566 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003572 | CCTGGGGGCGGCGCC[A/G]TCTCCTCTGGGTGGG | 79058 |
| rs778443636 | snp | A/T | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979163 | ACTCAGCAGTTCACC[A/T]TCCTTTCATCTCACC | 79058 |
| rs778459351 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985174 | CACACCTGCACACAC[C/G]CACACACCAACATGC | 79058 |
| rs778499219 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81990020 | GGTCAGGTGATCAGC[C/G]CGCCTCGGCCTCCCA | 79058 |
| rs778534351 | snp | A/T | 2.48419e-05 | 0.00352425 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996090 | GTGCTGCTGGGGCCG[A/T]GGAGTCTATTTAGCT | 79058 |
| rs778536648 | snp | C/T | 4.43715e-05 | 0.00470997 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009174 | GAGAAGACGCTTGGC[C/T]CAGCTCAAGAGTGAG | 79058 |
| rs778538835 | snp | C/T | 5.00663e-05 | 0.00500307 | downstream-variant-500B, intron-variant, synonymous-codon | ASPSCR1 | GRCh38.p7 | 17:82017449 | AAGGGCCCCCGTCGT[C/T]TGCCCTGGCTCAGCT | 79058 |
| rs778617770 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006922 | CTGCCGCTGTGGCTC[C/T]CCCTTCCTGGCCCCT | 79058 |
| rs778619894 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81993037 | GATGCCCCTCCCCCA[A/G]GATTGAGGACGTGAA | 79058 |
| rs778625155 | snp | A/G | 5.71488e-05 | 0.0053452 | missense, utr-variant-5-prime, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983573 | CAGAGGAGCGTGCTC[A/G]ACCTTTCTCTCCAGT | 79058 |
| rs778684086 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002192 | TTCTTTTTAAAATTA[A/G]AAAGTGATTTTTTTT | 79058 |
| rs778710068 | snp | A/G | | | | | GRCh38.p7 | 17:82006194 | GGTGTGTGTGTGTGC[A/G]TCCTTGCATGTGCAC | 79058 |
| rs778824296 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81997216 | GTGGCACAGAGCAGG[A/G]CCGCCCTGGGGTGGT | 79058 |
| rs778958694 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982807 | CTTTTCTTTTCTTTT[C/G]TTTCCTTTCCTTTCC | 79058 |
| rs778978508 | snp | A/G/T | 6.94208e-05 | 0.0058912 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012174 | TGTCTTCCTTCGGGC[A/G/T]CATGGATGGGCGAGG | 79058 |
| rs778982611 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996584 | ACACCTCAGGGCCCT[A/G]CTGCGAGCACACTCA | 79058 |
| rs779033384 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979247 | GATCTGAAGTGAGTT[C/T]GCTCCAGCTCAGCAG | 79058 |
| rs779058676 | snp | C/G | 5.114e-05 | 0.00505642 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82017011 | CCTAAGTCTGAGCCA[C/G]CTGCTGAGGAGGGGG | 79058 |
| rs779076189 | snp | C/T | 9.98253e-05 | 0.00706418 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010825 | GAGGGTCCTGTTCCC[C/T]GACCGCTACGTCCTA | 79058 |
| rs779117954 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987354 | TGCTGCTTCCTGAGA[C/T]GAGAGTGGCAGAGGG | 79058 |
| rs779121131 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981444 | AGTACAGTGGCGCTA[G/T]CTCGGCTCACTGCAA | 79058 |
| rs779195074 | snp | C/G/T | 8.94408e-05 | 0.00668684 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015202 | ACTCTGGGAGGCTTC[C/G/T]TTTTTGGGGTCCATC | 79058 |
| rs779202825 | snp | A/C | 2.28058e-05 | 0.00337674 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009618 | GCTCTGAGGGGGCCC[A/C]CCGTGAGGTCTGTGG | 79058 |
| rs779224625 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81976768 | GTGCGAGTGCTGTCC[A/T]TGAGTGGCCCAGGTG | 79058 |
| rs779251883 | snp | C/G | 1.79735e-05 | 0.00299774 | missense, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015132 | TCGCTGAAACGGTGC[C/G]TGGGACCAGAGCAGA | 79058 |
| rs779278268 | snp | C/T | 1.64874e-05 | 0.00287113 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979147 | CCCGCCAGCCCTGCA[C/T]ACTCAGCAGTTCACC | 79058 |
| rs779283181 | snp | C/G | 4.5881e-05 | 0.00478941 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977679 | CGGCGGAGGCTCCGC[C/G]GTGTCGGTGCTGGCC | 79058 |
| rs779291808 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81978090 | CCTAGACCCGCGTTC[C/T]CATTCCGGGGCGTCC | 79058 |
| rs779308459 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011488 | CAGGTGCTGGGGCAG[-/C]CCCGGGGCTGGCGTG | 79058 |
| rs779342593 | snp | C/T | 1.67733e-05 | 0.00289592 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017284 | GCCCGGGGTGTGTGG[C/T]CACCCTGATGTGTCT | 79058 |
| rs779347171 | snp | A/G | | | upstream-variant-2KB, nc-transcript-variant | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81975928 | AGGGGAAGCTTGACC[A/G]AAAGTGACTATAAAT | 79058 |
| rs779405475 | in-del | -/G | 0.000118811 | 0.00770659 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010897 | GGGGTGTCCGGGGAT[-/G]GGGGGGCAGGGGCCC | 79058 |
| rs779440611 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999261 | GGGCCAGGTCAGAGC[G/T]TCTTGAGCTCCTGCT | 79058 |
| rs779527859 | in-del | -/TGGCTGGGCACAG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986130 | CTAATAGTAATTGGA[-/TGGCTGGGCACAG]TGGCTGGGCACAGTG | 79058 |
| rs779528690 | snp | A/G | 3.33745e-05 | 0.00408487 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012317 | GGGGTGCTGCGGGGC[A/G]GGGCCCTCCAGGGAG | 79058 |
| rs779553257 | snp | C/T | 1.64822e-05 | 0.00287068 | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979263 | GCTCCAGCTCAGCAG[C/T]AGGGTCTGAGTATAT | 79058 |
| rs779556818 | snp | A/G | 3.63888e-05 | 0.00426533 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995017 | GACGTGTTTCATGGA[A/G]AAAGAGGGAGTGGCC | 79058 |
| rs779650888 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003762 | CTCCCCACAGAGCCC[A/G]CGCCCACGCCCTGGC | 79058 |
| rs779658040 | in-del | -/AA | 0.000267046 | 0.0115521 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996106 | GGAGTCTATTTAGCT[-/AA]AAAAAAAAGTGGTCT | 79058 |
| rs779663245 | snp | C/T | 1.79606e-05 | 0.00299666 | synonymous-codon, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015305 | CCCTCGTCCGAGCAG[C/T]GGCGATCCCTCCCGA | 79058 |
| rs779740951 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015956 | AGGCTGAGGTTTCGG[C/T]GTTCCTGGGCCTGGC | 79058 |
| rs779747467 | snp | C/T | 7.9621e-05 | 0.00630905 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995965 | TCCCGGTGCAAGGCG[C/T]ACCTGTCCTGGCTGC | 79058 |
| rs779775512 | snp | G/T | 2.01298e-05 | 0.00317246 | intron-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82012156 | CACCCCCATCTGCAG[G/T]CCTGTCTTCCTTCGG | 79058 |
| rs779808008 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983362 | TTCTGCTTGCAGGAG[A/G]CCCCATATGATCGGG | 79058 |
| rs779819197 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81991091 | CAAGGGTGAGCCGTG[A/G]GAACTCACACAGCAG | 79058 |
| rs779910956 | snp | A/G | 8.45444e-05 | 0.00650116 | utr-variant-3-prime, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017357 | CCCACTCCGCCAGCC[A/G]CAGGACCACCTCCTC | 79058 |
| rs779933572 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008147 | GTACCTCTGGCAGGC[A/G]CACCCTGGCTGTCAC | 79058 |
| rs779978070 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010384 | AATACAAAAAATTAG[C/T]CAGGAGAGGTGGCGC | 79058 |
| rs780091473 | snp | A/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015639 | TGTGCCCACAGCAGC[A/C]TCTGGGCAGTGTACC | 79058 |
| rs780143205 | snp | A/G | 1.6661e-05 | 0.00288621 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010766 | CCCTGGTGCAGCTCC[A/G]GCCGTCCCTCCAACC | 79058 |
| rs780191032 | snp | G/T | 1.72621e-05 | 0.00293781 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996517 | AGCGCTCCACTTCCC[G/T]TGGAATCTGGGGAGC | 79058 |
| rs780193631 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007095 | CAGACGCCATATGTT[C/G]TCGGGGTGACTCAGG | 79058 |
| rs780194598 | snp | C/T | 3.33439e-05 | 0.00408299 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985488 | CCTAAGGAAGTTTCT[C/T]ATGTCTTATACCCTC | 79058 |
| rs780242386 | snp | A/G | 1.72178e-05 | 0.00293404 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996461 | TGGGCAAGACCCCAG[A/G]AAGCCTGGGCTCGTC | 79058 |
| rs780278849 | snp | A/G | 2.05746e-05 | 0.00320732 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977639 | GCGGCGGGTCACGTG[A/G]GCGGAAAATGGCGGC | 79058 |
| rs780290173 | in-del | -/CGCCTG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82003833 | GTCCACGTGCTCCGC[-/CGCCTG]CCTCCGAGGGTGGCC | 79058 |
| rs780398862 | snp | C/T | 4.36891e-05 | 0.00467361 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994953 | GAAAATCTGCTGTCC[C/T]GCAGCCGTCTCCAGG | 79058 |
| rs780426058 | snp | A/G | 2.14526e-05 | 0.00327503 | synonymous-codon, nc-transcript-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017112 | GTGGCTGAAGCTGCC[A/G]GGTACTGCGGCTGGG | 79058 |
| rs780435022 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81987427 | GATGAACGTCTGGAA[A/G]GAAATGCCCCTGGGC | 79058 |
| rs780449927 | in-del | -/C | 1.85513e-05 | 0.00304554 | intron-variant, frameshift-variant | ASPSCR1 | GRCh38.p7 | 17:82012165 | CTGCAGGCCTGTCTT[-/C]CTTCGGGCGCATGGA | 79058 |
| rs780467570 | snp | A/G | 1.67688e-05 | 0.00289554 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996688 | GGCCCTCCTGGGCCC[A/G]CGAGGCCTCTGACAT | 79058 |
| rs780500663 | snp | A/G | 0.000101621 | 0.00712742 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82009062 | GGGAGCCCGTGGACC[A/G]GGAGCCGGTGGTGTG | 79058 |
| rs780568246 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81989024 | ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCGTC | 79058 |
| rs780598772 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82005030 | CAGGGGAGGCCATCC[A/G]TGGCTGGGCGAGGGT | 79058 |
| rs780601115 | snp | C/T | 3.39934e-05 | 0.00412256 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996773 | CAAAGAAGTCCAAGT[C/T]GGGCCAGGATCCCCA | 79058 |
| rs780777895 | snp | C/T | 0.000569314 | 0.0168622 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995039 | GGAGTGGCCGGCCCT[C/T]GGAGCCCGGGCTGCC | 79058 |
| rs780782841 | snp | C/T | 1.67784e-05 | 0.00289636 | synonymous-codon, nc-transcript-variant, missense | ASPSCR1 | GRCh38.p7 | 17:82017310 | TGTCTGCACTACAGC[C/T]AGCAAGAGGTGAGAG | 79058 |
| rs780837494 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013584 | AAGCACCAGCTTTCA[C/T]GTCTCTGGCAGAGCC | 79058 |
| rs780883351 | snp | C/T | 2.22126e-05 | 0.00333254 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008986 | TGACAGCCCGGGGTG[C/T]GGAGGGCCCAGCCCG | 79058 |
| rs780920234 | snp | A/G | 5.05898e-05 | 0.00502915 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82016849 | CATCTCCCCATCTGC[A/G]GCCGATGTGCTGGTG | 79058 |
| rs780936267 | snp | A/C | 1.67214e-05 | 0.00289144 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011639 | GCCCACTCCTGCCTC[A/C]AGTGCTCGGGGCCTT | 79058 |
| rs780941381 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81982354 | ATTTTGAGGCAGGTC[C/T]TGCAATACCATAGCC | 79058 |
| rs780973405 | snp | A/G | 2.2771e-05 | 0.00337416 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82016749 | GATGCTGGGTGGATG[A/G]TGAGTGGACCCCTCC | 79058 |
| rs780994739 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81981638 | CCCGCCTTGGTCTTC[C/T]AAAGTGTTGGGATTA | 79058 |
| rs781017976 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986137 | TAATTGGATGGCTGG[C/G]CACAGTGGCTGGGCA | 79058 |
| rs781040234 | snp | C/T | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017602 | TATTTACACTTCCTC[C/T]AAGGAGAACAGAAGT | 79058 |
| rs781083505 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012152 | GCGTCACCCCCATCT[G/T]CAGGCCTGTCTTCCT | 79058 |
| rs781103409 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81980045 | TGGAGTGCAGTGGCA[C/T]GGTCTTGGCTCACTG | 79058 |
| rs781122032 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81999578 | GTTGCAGTGAGCCGA[G/T]ATCGTGCCACTGCAC | 79058 |
| rs781146459 | snp | C/T | 4.08338e-05 | 0.00451832 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015037 | TCCCGGGCCCTGCTC[C/T]GGCTGGGGGGACGGT | 79058 |
| rs781180255 | snp | A/G | 6.29862e-05 | 0.00561152 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81983662 | CCGTGAGGGGCCTGA[A/G]AACATGGTGGGTCGT | 79058 |
| rs781194888 | snp | A/G | 2.10644e-05 | 0.00324527 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81977624 | TTTGACGCCGGCCCG[A/G]CGGCGGGTCACGTGA | 79058 |
| rs781228809 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81985383 | CTTCTCCGTGGGGGT[C/T]AGCCTCTCCCTGGAG | 79058 |
| rs781269043 | snp | A/C | 1.76524e-05 | 0.00297084 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996441 | CATGAAGTGCTACGA[A/C]CCCGTGGGCAAGACC | 79058 |
| rs781327542 | snp | A/G | 1.88081e-05 | 0.00306655 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81996372 | GGGAGAGGGTGAGCC[A/G]GGGGTAGGCACCACA | 79058 |
| rs781327687 | snp | C/T | 1.67405e-05 | 0.00289309 | missense, nc-transcript-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009559 | GAGAAGCTGGAGCGC[C/T]ACCCAAAGGTCTGCA | 79058 |
| rs781329050 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81995174 | GATCATTTTCAAAAC[C/T]GAGTGTGGCGTGGCG | 79058 |
| rs781337294 | snp | A/G | 2.03126e-05 | 0.00318683 | stop-gained, nc-transcript-variant, intron-variant | ASPSCR1 | GRCh38.p7 | 17:82017099 | GCAAGGTGCCCAAGT[A/G]GCTGAAGCTGCCGGG | 79058 |
| rs781354321 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82008256 | GGGTAGACGGGACGG[A/G]ACCAGGAGGGTTGTT | 79058 |
| rs781378946 | snp | C/G | 8.921e-05 | 0.0066781 | intron-variant, downstream-variant-500B | ASPSCR1 | GRCh38.p7 | 17:82009470 | GAAGCCCTGTTCCTT[C/G]CCCTCCTCACCACAG | 79058 |
| rs781391940 | snp | A/G | 1.8581e-05 | 0.00304797 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81994934 | TCAGCCCACTTTCCA[A/G]CTGGAAAATCTGCTG | 79058 |
| rs781443683 | snp | C/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014860 | TGTCCTGGGCGGCAG[C/G]TAGGGAGGGGCCGGC | 79058 |
| rs781445169 | snp | A/G | 3.3355e-05 | 0.00408367 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81994843 | CTGCAGCACCCCGGC[A/G]GGGCCACCCCAGTCT | 79058 |
| rs781448157 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007174 | CAGCGAGGCTGCTCC[A/G]GATCGGGGCTGCTCT | 79058 |
| rs781487640 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015854 | CCCACAGGCCCTTCT[C/T]TGCTCACAAGGCTTT | 79058 |
| rs781499101 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983277 | CACTGGGGCTGTCAG[C/T]ACCCCAGACTCTGAA | 79058 |
| rs781521700 | in-del | -/G | 4.03934e-05 | 0.00449389 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82015041 | GGCCCTGCTCTGGCT[-/G]GGGGGGACGGTGTGA | 79058 |
| rs781535767 | snp | C/G | 1.70252e-05 | 0.00291759 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996607 | CACACTCAGGAGAAG[C/G]AGAGCACAAGGGCAC | 79058 |
| rs781568005 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82000923 | CACAACTCGGCCTCC[C/T]GGCAGCTGGCACGAG | 79058 |
| rs781581806 | snp | A/C/G | 3.35882e-05 | 0.00409795 | missense, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:81996674 | GACAGAGACTGGGGG[A/C/G]CCCTCCTGGGCCCAC | 79058 |
| rs781589037 | snp | C/T | 1.66746e-05 | 0.00288739 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82010849 | CGTCCTACAGGGCTT[C/T]TTCCGCCCCAGCGAG | 79058 |
| rs781627131 | snp | C/T | 4.98442e-05 | 0.00499196 | synonymous-codon, nc-transcript-variant | ASPSCR1 | GRCh38.p7 | 17:82012274 | CGACCACACGCAGAC[C/T]CTCTTTCAGGTACCT | 79058 |
| rs781637310 | snp | G/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007557 | CTGGACGTGGCCGCC[G/T]GAGCACGGCATGTCC | 79058 |
| rs781689247 | snp | C/T | | | intron-variant, upstream-variant-2KB | ASPSCR1, LOC105371939 | GRCh38.p7 | 17:81979349 | TTTTAAACAGTCATA[C/T]ATTCCCTCCCAACTC | 79058 |
| rs781715032 | snp | A/G | 0.000102708 | 0.00716544 | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010909 | GGATGGGGGGCAGGG[A/G]CCCATGGGGCCTCTC | 79058 |
| rs796147751 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009801 | CCCCCTGTGAGGTCT[A/G]TGGATGGGACGTGGG | 79058 |
| rs796183618 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983090 | CCTCAGGTGATCCGC[C/T]TGCCTCGGCCTCCGA | 79058 |
| rs796263502 | in-del | -/C | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81984995 | ACACCTGCGTGCACA[-/C]CCCCCCACACACCTG | 79058 |
| rs796352234 | multinucleotide-polymorphism | AC/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009630 | CCCCCGTGAGGTCTG[AC/GT]GACGGGATGGGGCGA | 79058 |
| rs796371172 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82011834 | TGCCTTCTCTCTCAG[C/T]GCCCTGCTCCCCTCT | 79058 |
| rs796388849 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82014288 | GGCCTCTCTGGGACC[A/G]ACAGGCCCCCTTCCT | 79058 |
| rs796412513 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983310 | AGCAGCCCCCTCGGC[A/G]TGCACCGAGGCCCAC | 79058 |
| rs796439978 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81986771 | AAGGTGACTGTGCGT[C/T]GGGCGCGCTTGGTGG | 79058 |
| rs796632381 | in-del | -/GGATGGCGGGGCGT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:81983480 | TGGATGGTGGGACGG[-/GGATGGCGGGGCGT]GGATGGCGGGGCGTG | 79058 |
| rs796679159 | snp | A/G | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82012461 | AGTTGCTTCTGACAC[A/G]GCTTTCCGGCCTCCT | 79058 |
| rs796723689 | snp | C/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82007178 | GAGGCTGCTCCGGAT[C/T]GGGGCTGCTCTGCCC | 79058 |
| rs796732200 | multinucleotide-polymorphism | AC/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010344 | CCATCCTGGCTGACA[AC/GT]GTGAAACCCCATCTC | 79058 |
| rs796774503 | in-del | -/CT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82009915 | GATTTAGAATGAAAC[-/CT]TTTTTTTTTTTTGAG | 79058 |
| rs796784803 | in-del | -/GT | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82006230 | TGTGTGTGTGTGTGT[-/GT]CCTTGCGGGTGCATG | 79058 |
| rs796836095 | snp | A/G | | | downstream-variant-500B, intron-variant, utr-variant-3-prime | ASPSCR1 | GRCh38.p7 | 17:82017861 | AACTGACCTACTGAG[A/G]TGGGCAGGGCGGGGA | 79058 |
| rs796845452 | in-del | -/T | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82002881 | TCTTTTTAAAATAAC[-/T]TTTTTTTTTTCGAGA | 79058 |
| rs796880412 | multinucleotide-polymorphism | CA/TG | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82010340 | GAGACCATCCTGGCT[CA/TG]CACGGTGAAACCCCA | 79058 |
| rs796906867 | in-del | -/TGCC | | | intron-variant | ASPSCR1 | GRCh38.p7 | 17:82013480 | GTGTCCCCGGTGACG[-/TGCC]TGCCTGCCTGCCTGC | 79058 |